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Erschienen in: Pediatric Radiology 2/2021

06.10.2020 | Review

Imaging of Horner syndrome in pediatrics: association with neuroblastoma

verfasst von: Hedieh Khalatbari, Gisele E. Ishak

Erschienen in: Pediatric Radiology | Ausgabe 2/2021

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Abstract

Neuroblastoma is the most common neoplasm associated with pediatric Horner syndrome. The laboratory and imaging evaluation of isolated pediatric Horner syndrome is controversial. We review the literature published in the last several decades and present the rationale for the imaging work-up in this patient cohort.
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Literatur
1.
Zurück zum Zitat Karemaker JM (2017) An introduction into autonomic nervous function. Physiol Meas 38:R89–R118PubMed Karemaker JM (2017) An introduction into autonomic nervous function. Physiol Meas 38:R89–R118PubMed
3.
Zurück zum Zitat Gross JR, McClelland CM, Lee MS (2016) An approach to anisocoria. Curr Opin Ophthalmol 27:486–492PubMed Gross JR, McClelland CM, Lee MS (2016) An approach to anisocoria. Curr Opin Ophthalmol 27:486–492PubMed
4.
Zurück zum Zitat Martin TJ (2018) Horner syndrome: a clinical review. ACS Chem Neurosci 9:177–186PubMed Martin TJ (2018) Horner syndrome: a clinical review. ACS Chem Neurosci 9:177–186PubMed
5.
Zurück zum Zitat Smith SJ, Diehl N, Leavitt JA, Mohney BG (2010) Incidence of pediatric Horner syndrome and the risk of neuroblastoma: a population-based study. Arch Ophthalmol 128:324–329PubMedPubMedCentral Smith SJ, Diehl N, Leavitt JA, Mohney BG (2010) Incidence of pediatric Horner syndrome and the risk of neuroblastoma: a population-based study. Arch Ophthalmol 128:324–329PubMedPubMedCentral
6.
Zurück zum Zitat Abbas A, Manjila S, Singh M et al (2015) Johann Friedrich Horner and the repeated discovery of oculosympathoparesis: whose syndrome is it? Neurosurgery 77:486–491PubMed Abbas A, Manjila S, Singh M et al (2015) Johann Friedrich Horner and the repeated discovery of oculosympathoparesis: whose syndrome is it? Neurosurgery 77:486–491PubMed
7.
Zurück zum Zitat Wilhelm H (2011) Disorders of the pupil. Handb Clin Neurol 102:427–466PubMed Wilhelm H (2011) Disorders of the pupil. Handb Clin Neurol 102:427–466PubMed
8.
Zurück zum Zitat Cohen LM, Elliott A, Freitag SK (2018) Acquired intermittent pediatric Horner syndrome due to neuroblastoma. Ophthalmic Plast Reconstr Surg 34:e38–e41PubMed Cohen LM, Elliott A, Freitag SK (2018) Acquired intermittent pediatric Horner syndrome due to neuroblastoma. Ophthalmic Plast Reconstr Surg 34:e38–e41PubMed
9.
Zurück zum Zitat Albert DM, Rubenstein RA, Scheie HG (1967) Tumor metastasis to the eye. II. Clinical study in infants and children. Am J Ophthalmol 63:727–732PubMed Albert DM, Rubenstein RA, Scheie HG (1967) Tumor metastasis to the eye. II. Clinical study in infants and children. Am J Ophthalmol 63:727–732PubMed
10.
Zurück zum Zitat Jaffe N, Cassady R, Petersen R, Traggis D (1975) Heterochromia and Horner syndrome associated with cervical and mediastinal neuroblastoma. J Pediatr 87:75–77PubMed Jaffe N, Cassady R, Petersen R, Traggis D (1975) Heterochromia and Horner syndrome associated with cervical and mediastinal neuroblastoma. J Pediatr 87:75–77PubMed
11.
Zurück zum Zitat McRae D Jr, Shaw A (1979) Ganglioneuroma, heterochromia iridis, and Horner’s syndrome. J Pediatr Surg 14:612–614PubMed McRae D Jr, Shaw A (1979) Ganglioneuroma, heterochromia iridis, and Horner’s syndrome. J Pediatr Surg 14:612–614PubMed
12.
Zurück zum Zitat Sayed AK, Miller BA, Lack EE et al (1983) Heterochromia iridis and Horner's syndrome due to paravertebral neurilemmoma. J Surg Oncol 22:15–16PubMed Sayed AK, Miller BA, Lack EE et al (1983) Heterochromia iridis and Horner's syndrome due to paravertebral neurilemmoma. J Surg Oncol 22:15–16PubMed
13.
Zurück zum Zitat O’Glasser AY, Milas KM (2016) Horner’s, heterochromia, and harlequins. J Gen Intern Med 31:137PubMed O’Glasser AY, Milas KM (2016) Horner’s, heterochromia, and harlequins. J Gen Intern Med 31:137PubMed
14.
Zurück zum Zitat Morrison DA, Bibby K, Woodruff G (1997) The “harlequin” sign and congenital Horner’s syndrome. J Neurol Neurosurg Psychiatry 62:626–628PubMedPubMedCentral Morrison DA, Bibby K, Woodruff G (1997) The “harlequin” sign and congenital Horner’s syndrome. J Neurol Neurosurg Psychiatry 62:626–628PubMedPubMedCentral
15.
16.
Zurück zum Zitat Braungart S, Craigie RJ, Farrelly P, Losty PD (2019) Paediatric Horner’s syndrome: is investigation for underlying malignancy always required? Arch Dis Child 104:984–987PubMed Braungart S, Craigie RJ, Farrelly P, Losty PD (2019) Paediatric Horner’s syndrome: is investigation for underlying malignancy always required? Arch Dis Child 104:984–987PubMed
17.
Zurück zum Zitat Loewenfeld IE (1977) “Simple central” anisocoria: a common condition, seldom recognized. Trans Sect Ophthalmol Am Acad Ophthalmol Otolaryngol 83:832–839PubMed Loewenfeld IE (1977) “Simple central” anisocoria: a common condition, seldom recognized. Trans Sect Ophthalmol Am Acad Ophthalmol Otolaryngol 83:832–839PubMed
18.
Zurück zum Zitat Lam BL, Thompson HS, Corbett JJ (1987) The prevalence of simple anisocoria. Am J Ophthalmol 104:69–73PubMed Lam BL, Thompson HS, Corbett JJ (1987) The prevalence of simple anisocoria. Am J Ophthalmol 104:69–73PubMed
19.
Zurück zum Zitat Reede DL, Garcon E, Smoker WRK, Kardon R (2008) Horner’s syndrome: clinical and radiographic evaluation. Neuroimaging Clin N Am 18:369–385, xi Reede DL, Garcon E, Smoker WRK, Kardon R (2008) Horner’s syndrome: clinical and radiographic evaluation. Neuroimaging Clin N Am 18:369–385, xi
20.
Zurück zum Zitat Barrea C, Vigouroux T, Karam J et al (2016) Horner syndrome in children: a clinical condition with serious underlying disease. Neuropediatrics 47:268–272PubMed Barrea C, Vigouroux T, Karam J et al (2016) Horner syndrome in children: a clinical condition with serious underlying disease. Neuropediatrics 47:268–272PubMed
21.
Zurück zum Zitat Nagy AN, Hayman LA, Diaz-Marchan PJ, Lee AG (1997) Horner’s syndrome due to first-order neuron lesions of the oculosympathetic pathway. AJR Am J Roentgenol 169:581–584PubMed Nagy AN, Hayman LA, Diaz-Marchan PJ, Lee AG (1997) Horner’s syndrome due to first-order neuron lesions of the oculosympathetic pathway. AJR Am J Roentgenol 169:581–584PubMed
22.
Zurück zum Zitat George A, Haydar AA, Adams WM (2008) Imaging of Horner’s syndrome. Clin Radiol 63:499–505PubMed George A, Haydar AA, Adams WM (2008) Imaging of Horner’s syndrome. Clin Radiol 63:499–505PubMed
23.
Zurück zum Zitat Giles CL, Henderson JW (1958) Horner’s syndrome: an analysis of 216 cases. Am J Ophthalmol 46:289–296PubMed Giles CL, Henderson JW (1958) Horner’s syndrome: an analysis of 216 cases. Am J Ophthalmol 46:289–296PubMed
24.
Zurück zum Zitat George ND, Gonzalez G, Hoyt CS (1998) Does Horner’s syndrome in infancy require investigation? Br J Ophthalmol 82:51–54PubMedPubMedCentral George ND, Gonzalez G, Hoyt CS (1998) Does Horner’s syndrome in infancy require investigation? Br J Ophthalmol 82:51–54PubMedPubMedCentral
25.
Zurück zum Zitat Ben Shabat A, Ash S, Luckman J et al (2019) Likelihood of diagnosing neuroblastoma in isolated Horner syndrome. J Neuroophthalmol 39:308–312PubMed Ben Shabat A, Ash S, Luckman J et al (2019) Likelihood of diagnosing neuroblastoma in isolated Horner syndrome. J Neuroophthalmol 39:308–312PubMed
26.
Zurück zum Zitat Robertson WC, Pettigrew LC (2003) “Congenital” Horner’s syndrome and carotid dissection. J Neuroimaging 13:367–370PubMed Robertson WC, Pettigrew LC (2003) “Congenital” Horner’s syndrome and carotid dissection. J Neuroimaging 13:367–370PubMed
27.
Zurück zum Zitat Gupta M, Dinakaran S, Chan TK (2005) Congenital Horner syndrome and hemiplegia secondary to carotid dissection. J Pediatr Ophthalmol Strabismus 42:122–124PubMed Gupta M, Dinakaran S, Chan TK (2005) Congenital Horner syndrome and hemiplegia secondary to carotid dissection. J Pediatr Ophthalmol Strabismus 42:122–124PubMed
28.
Zurück zum Zitat Beckerman BL, Seaver R (1978) Congenital Horner’s syndrome and thoracic neuroblastoma. J Pediatr Ophthalmol Strabismus 15:24–25PubMed Beckerman BL, Seaver R (1978) Congenital Horner’s syndrome and thoracic neuroblastoma. J Pediatr Ophthalmol Strabismus 15:24–25PubMed
29.
Zurück zum Zitat Musarella MA, Chan HS, DeBoer G, Gallie BL (1984) Ocular involvement in neuroblastoma: prognostic implications. Ophthalmology 91:936–940PubMed Musarella MA, Chan HS, DeBoer G, Gallie BL (1984) Ocular involvement in neuroblastoma: prognostic implications. Ophthalmology 91:936–940PubMed
30.
Zurück zum Zitat Jeffery AR, Ellis FJ, Repka MX, Buncic JR (1998) Pediatric Horner syndrome. J AAPOS 2:159–167PubMed Jeffery AR, Ellis FJ, Repka MX, Buncic JR (1998) Pediatric Horner syndrome. J AAPOS 2:159–167PubMed
31.
Zurück zum Zitat Zafeiriou DI, Economou M, Koliouskas D et al (2006) Congenital Horner’s syndrome associated with cervical neuroblastoma. Eur J Paediatr Neurol 10:90–92PubMed Zafeiriou DI, Economou M, Koliouskas D et al (2006) Congenital Horner’s syndrome associated with cervical neuroblastoma. Eur J Paediatr Neurol 10:90–92PubMed
32.
Zurück zum Zitat Kadom N, Rosman NP, Jubouri S et al (2015) Neuroimaging experience in pediatric Horner syndrome. Pediatr Radiol 45:1535–1543PubMed Kadom N, Rosman NP, Jubouri S et al (2015) Neuroimaging experience in pediatric Horner syndrome. Pediatr Radiol 45:1535–1543PubMed
33.
Zurück zum Zitat Martin GC, Aymard P-A, Denier C et al (2017) Usefulness of cocaine drops in investigating infant anisocoria. Eur J Paediatr Neurol 21:852–857PubMed Martin GC, Aymard P-A, Denier C et al (2017) Usefulness of cocaine drops in investigating infant anisocoria. Eur J Paediatr Neurol 21:852–857PubMed
34.
Zurück zum Zitat Ott C, Bobylev A, Holland-Cunz SG, Mayr J (2018) Unilateral straight hair-a symptom of acquired Horner’s syndrome in a neonate. European J Pediatr Surg Rep 6:e32–e36PubMedPubMedCentral Ott C, Bobylev A, Holland-Cunz SG, Mayr J (2018) Unilateral straight hair-a symptom of acquired Horner’s syndrome in a neonate. European J Pediatr Surg Rep 6:e32–e36PubMedPubMedCentral
35.
Zurück zum Zitat Berroth ML, Morozova LV, Pollock JM (2020) Ectopic thymus as a cause of Horner’s syndrome. Radiol Case Rep 15:23–25PubMed Berroth ML, Morozova LV, Pollock JM (2020) Ectopic thymus as a cause of Horner’s syndrome. Radiol Case Rep 15:23–25PubMed
36.
37.
Zurück zum Zitat Deprez FC, Coulier J, Rommel D, Boschi A (2015) Congenital Horner syndrome with heterochromia iridis associated with ipsilateral internal carotid artery hypoplasia. J Clin Neurol 11:192–196PubMed Deprez FC, Coulier J, Rommel D, Boschi A (2015) Congenital Horner syndrome with heterochromia iridis associated with ipsilateral internal carotid artery hypoplasia. J Clin Neurol 11:192–196PubMed
38.
Zurück zum Zitat Ryan F-H, Kline LB, Gomez C (2000) Congenital Horner’s syndrome resulting from agenesis of the internal carotid artery. Ophthalmology 107:185–188PubMed Ryan F-H, Kline LB, Gomez C (2000) Congenital Horner’s syndrome resulting from agenesis of the internal carotid artery. Ophthalmology 107:185–188PubMed
39.
Zurück zum Zitat Dinc H, Alioglu Z, Erdol H, Ahmetoglu A (2002) Agenesis of the internal carotid artery associated with aortic arch anomaly in a patient with congenital Horner’s syndrome. AJNR Am J Neuroradiol 23:929–931PubMed Dinc H, Alioglu Z, Erdol H, Ahmetoglu A (2002) Agenesis of the internal carotid artery associated with aortic arch anomaly in a patient with congenital Horner’s syndrome. AJNR Am J Neuroradiol 23:929–931PubMed
40.
Zurück zum Zitat Fons C, Vasconcelos M, Vidal M et al (2009) Agenesis of internal carotid artery in a child with ipsilateral Horner’s syndrome. J Child Neurol 24:101–104PubMed Fons C, Vasconcelos M, Vidal M et al (2009) Agenesis of internal carotid artery in a child with ipsilateral Horner’s syndrome. J Child Neurol 24:101–104PubMed
41.
Zurück zum Zitat Cagan E, Sayin R, Dogan M et al (2010) Bilateral brachial plexus palsy and right Horner syndrome due to congenital cervicothoracal syringomyelia. Brain Dev 32:595–597 Cagan E, Sayin R, Dogan M et al (2010) Bilateral brachial plexus palsy and right Horner syndrome due to congenital cervicothoracal syringomyelia. Brain Dev 32:595–597
42.
Zurück zum Zitat Jurca MC, Kozma K, Petchesi CD et al (2017) Anatomic variants in Dandy-Walker complex. Romanian J Morphol Embryol 58:1051–1055 Jurca MC, Kozma K, Petchesi CD et al (2017) Anatomic variants in Dandy-Walker complex. Romanian J Morphol Embryol 58:1051–1055
43.
Zurück zum Zitat Lee N, Nam S-O, Kim YM, Lee Y-J (2016) A neonate with Joubert syndrome presenting with symptoms of Horner syndrome. Korean J Pediatr 59:S32–S36PubMedPubMedCentral Lee N, Nam S-O, Kim YM, Lee Y-J (2016) A neonate with Joubert syndrome presenting with symptoms of Horner syndrome. Korean J Pediatr 59:S32–S36PubMedPubMedCentral
44.
Zurück zum Zitat Puvanachandra N, Heran MK, Lyons CJ (2008) Morning glory disk anomaly with ipsilateral capillary hemangioma, agenesis of the internal carotid artery, and Horner syndrome: a variant of PHACES syndrome? J AAPOS 12:528–530PubMed Puvanachandra N, Heran MK, Lyons CJ (2008) Morning glory disk anomaly with ipsilateral capillary hemangioma, agenesis of the internal carotid artery, and Horner syndrome: a variant of PHACES syndrome? J AAPOS 12:528–530PubMed
45.
Zurück zum Zitat Sankaran A, Bhardwaj P, Venkatramani H, Sabapathy SR (2018) Birth palsy in congenital varicella syndrome: a lesson in anatomy. Indian J Plast Surg 51:238–242PubMedPubMedCentral Sankaran A, Bhardwaj P, Venkatramani H, Sabapathy SR (2018) Birth palsy in congenital varicella syndrome: a lesson in anatomy. Indian J Plast Surg 51:238–242PubMedPubMedCentral
46.
Zurück zum Zitat Naimer SA, Weinstein O, Rosenthal G (2000) Congenital Horner syndrome: a rare though significant complication of subclavian flap aortoplasty. J Thorac Cardiovasc Surg 120:419–421PubMed Naimer SA, Weinstein O, Rosenthal G (2000) Congenital Horner syndrome: a rare though significant complication of subclavian flap aortoplasty. J Thorac Cardiovasc Surg 120:419–421PubMed
47.
Zurück zum Zitat Woodruff G, Buncic JR, Morin JD (1988) Horner’s syndrome in children. J Pediatr Ophthalmol Strabismus 25:40–44PubMed Woodruff G, Buncic JR, Morin JD (1988) Horner’s syndrome in children. J Pediatr Ophthalmol Strabismus 25:40–44PubMed
48.
Zurück zum Zitat Massimi L, Pepa Della GM, Tamburrini G, Di Rocco C (2011) Sudden onset of Chiari malformation type I in previously asymptomatic patients. J Neurosurg Pediatr 8:438–442PubMed Massimi L, Pepa Della GM, Tamburrini G, Di Rocco C (2011) Sudden onset of Chiari malformation type I in previously asymptomatic patients. J Neurosurg Pediatr 8:438–442PubMed
49.
Zurück zum Zitat Shewmon DA (1983) Unilateral straight hair in congenital Horner syndrome due to stellate ganglion tumor. Ann Neurol 13:345–346PubMed Shewmon DA (1983) Unilateral straight hair in congenital Horner syndrome due to stellate ganglion tumor. Ann Neurol 13:345–346PubMed
50.
Zurück zum Zitat Gibbs J, Appleton RE, Martin J, Findlay G (1992) Congenital Horner syndrome associated with non-cervical neuroblastoma. Dev Med Child Neurol 34:642–644PubMed Gibbs J, Appleton RE, Martin J, Findlay G (1992) Congenital Horner syndrome associated with non-cervical neuroblastoma. Dev Med Child Neurol 34:642–644PubMed
51.
Zurück zum Zitat Moukheiber AK, Nicollas R, Roman S et al (2001) Primary pediatric neuroblastic tumors of the neck. Int J Pediatr Otorhinolaryngol 60:155–161PubMed Moukheiber AK, Nicollas R, Roman S et al (2001) Primary pediatric neuroblastic tumors of the neck. Int J Pediatr Otorhinolaryngol 60:155–161PubMed
52.
Zurück zum Zitat Mahoney NR, Liu GT, Menacker SJ et al (2006) Pediatric horner syndrome: etiologies and roles of imaging and urine studies to detect neuroblastoma and other responsible mass lesions. Am J Ophthalmol 142:651–659PubMed Mahoney NR, Liu GT, Menacker SJ et al (2006) Pediatric horner syndrome: etiologies and roles of imaging and urine studies to detect neuroblastoma and other responsible mass lesions. Am J Ophthalmol 142:651–659PubMed
53.
Zurück zum Zitat Pollard ZF, Greenberg MF, Bordenca M, Lange J (2010) Atypical acquired pediatric Horner syndrome. Arch Ophthalmol 128:937–940 Pollard ZF, Greenberg MF, Bordenca M, Lange J (2010) Atypical acquired pediatric Horner syndrome. Arch Ophthalmol 128:937–940
54.
Zurück zum Zitat Alvi S, Karadaghy O, Manalang M, Weatherly R (2017) Clinical manifestations of neuroblastoma with head and neck involvement in children. Int J Pediatr Otorhinolaryngol 97:157–162PubMed Alvi S, Karadaghy O, Manalang M, Weatherly R (2017) Clinical manifestations of neuroblastoma with head and neck involvement in children. Int J Pediatr Otorhinolaryngol 97:157–162PubMed
55.
Zurück zum Zitat Sauer C, Levingohn MW (1976) Horner’s syndrome in childhood. Neurology 26:216–220PubMed Sauer C, Levingohn MW (1976) Horner’s syndrome in childhood. Neurology 26:216–220PubMed
56.
Zurück zum Zitat Shikatani Y, Okazaki M, Sakao N et al (2015) A case of mediastinal granular cell tumor with Horner’s syndrome. Ann Thorac Cardiovasc Surg 21:567–569PubMedPubMedCentral Shikatani Y, Okazaki M, Sakao N et al (2015) A case of mediastinal granular cell tumor with Horner’s syndrome. Ann Thorac Cardiovasc Surg 21:567–569PubMedPubMedCentral
57.
Zurück zum Zitat Reid G, Purcell B, McNally O (2017) Metastatic testicular cancer, a Horner’s syndrome and brachial plexopathy. QJM 110:585–586PubMed Reid G, Purcell B, McNally O (2017) Metastatic testicular cancer, a Horner’s syndrome and brachial plexopathy. QJM 110:585–586PubMed
58.
Zurück zum Zitat Spors B, Seemann J, Homer N, Fay A (2017) Lymphatic malformation with acquired Horner syndrome in an infant. BMJ Case Rep 2017:bcr2017013315 Spors B, Seemann J, Homer N, Fay A (2017) Lymphatic malformation with acquired Horner syndrome in an infant. BMJ Case Rep 2017:bcr2017013315
59.
Zurück zum Zitat Watura K, Williams M, Bradley M (2015) Osteochondroma of the clavicle causing Horner’s syndrome. BMJ Case Rep 2015:bcr2015211705 Watura K, Williams M, Bradley M (2015) Osteochondroma of the clavicle causing Horner’s syndrome. BMJ Case Rep 2015:bcr2015211705
60.
Zurück zum Zitat Spector RH (2008) Postganglionic horner syndrome in three patients with coincident middle ear infection. J Neuroophthalmol 28:182–185PubMed Spector RH (2008) Postganglionic horner syndrome in three patients with coincident middle ear infection. J Neuroophthalmol 28:182–185PubMed
61.
Zurück zum Zitat Safran MJ, Greenwald MJ, Rice HC, Polin KS (1990) Cervical spine dislocation presenting as an isolated Horner’s syndrome. Arch Ophthalmol 108:327–328PubMed Safran MJ, Greenwald MJ, Rice HC, Polin KS (1990) Cervical spine dislocation presenting as an isolated Horner’s syndrome. Arch Ophthalmol 108:327–328PubMed
62.
Zurück zum Zitat Sohal APS, Dasarathi M, Gholkar A, McFarland R (2010) Unilateral Horner’s syndrome: an unusual childhood presentation. J Paediatr Child Health 46:695–701PubMed Sohal APS, Dasarathi M, Gholkar A, McFarland R (2010) Unilateral Horner’s syndrome: an unusual childhood presentation. J Paediatr Child Health 46:695–701PubMed
63.
Zurück zum Zitat Pirouzian A, Holz HA, Ip KC, Sudesh R (2010) Acquired infantile Horner syndrome and spontaneous internal carotid artery dissection: a case report and review of literature. J AAPOS 14:172–174PubMed Pirouzian A, Holz HA, Ip KC, Sudesh R (2010) Acquired infantile Horner syndrome and spontaneous internal carotid artery dissection: a case report and review of literature. J AAPOS 14:172–174PubMed
64.
Zurück zum Zitat Bayhan GI, Karaca M, Yazici U, Tanir G (2010) A case of Horner’s syndrome after the surgical treatment of pulmonary hydatid cyst. Turkiye Parazitol Derg 34:196–199PubMed Bayhan GI, Karaca M, Yazici U, Tanir G (2010) A case of Horner’s syndrome after the surgical treatment of pulmonary hydatid cyst. Turkiye Parazitol Derg 34:196–199PubMed
65.
Zurück zum Zitat Kumar KP, Alam MS (2018) “Collateral damage:” Horner’s syndrome following excision of a cervical vagal schwannoma. Int J Appl Basic Med Res 8:190–192PubMedPubMedCentral Kumar KP, Alam MS (2018) “Collateral damage:” Horner’s syndrome following excision of a cervical vagal schwannoma. Int J Appl Basic Med Res 8:190–192PubMedPubMedCentral
66.
Zurück zum Zitat van Santen HM, Aronson DC, Vulsma T et al (2004) Frequent adverse events after treatment for childhood-onset differentiated thyroid carcinoma: a single institute experience. Eur J Cancer 40:1743–1751PubMed van Santen HM, Aronson DC, Vulsma T et al (2004) Frequent adverse events after treatment for childhood-onset differentiated thyroid carcinoma: a single institute experience. Eur J Cancer 40:1743–1751PubMed
67.
Zurück zum Zitat Demiral M, Binay C, Simsek E, Ilhan H (2017) Horner syndrome secondary to thyroid surgery. Case Rep Endocrinol 2017:1689039PubMedPubMedCentral Demiral M, Binay C, Simsek E, Ilhan H (2017) Horner syndrome secondary to thyroid surgery. Case Rep Endocrinol 2017:1689039PubMedPubMedCentral
68.
Zurück zum Zitat Giannikas C, Pomeranz HD, Smith LP, Fefer Z (2014) Horner syndrome after tonsillectomy: an anatomic perspective. Pediatr Neurol 51:417–420PubMed Giannikas C, Pomeranz HD, Smith LP, Fefer Z (2014) Horner syndrome after tonsillectomy: an anatomic perspective. Pediatr Neurol 51:417–420PubMed
69.
Zurück zum Zitat Urfalioglu S, Acipayam C, Guler M et al (2020) A rare catheter complication in a patient with neuroblastoma: Horner’s syndrome. Ophthalmic Plast Reconstr Surg 36:e43–e44PubMed Urfalioglu S, Acipayam C, Guler M et al (2020) A rare catheter complication in a patient with neuroblastoma: Horner’s syndrome. Ophthalmic Plast Reconstr Surg 36:e43–e44PubMed
70.
Zurück zum Zitat Ghosh PS, Indulkar S (2012) Horner’s syndrome as complication of extracorporeal membrane oxygenation in a neonate. J Pediatr 160:349–349.e1PubMed Ghosh PS, Indulkar S (2012) Horner’s syndrome as complication of extracorporeal membrane oxygenation in a neonate. J Pediatr 160:349–349.e1PubMed
71.
Zurück zum Zitat Mutalib M, Vandervelde C, Varghese A et al (2007) Horner’s syndrome secondary to asymptomatic pneumothorax in an adolescent. Eur J Pediatr 166:507–508PubMed Mutalib M, Vandervelde C, Varghese A et al (2007) Horner’s syndrome secondary to asymptomatic pneumothorax in an adolescent. Eur J Pediatr 166:507–508PubMed
72.
Zurück zum Zitat Folkert KN, de Beaufort H, Bauman NM (2020) Horner syndrome from a pediatric otolaryngology perspective. Ann Otol Rhinol Laryngol 129:191–194PubMed Folkert KN, de Beaufort H, Bauman NM (2020) Horner syndrome from a pediatric otolaryngology perspective. Ann Otol Rhinol Laryngol 129:191–194PubMed
73.
Zurück zum Zitat Cebeci D, Arhan E, Demir E et al (2018) Internal carotid artery dissection without intracranial infarct following a minor shoulder trauma: the second pediatric case and review of the literature. J Clin Neurosci 56:172–175PubMed Cebeci D, Arhan E, Demir E et al (2018) Internal carotid artery dissection without intracranial infarct following a minor shoulder trauma: the second pediatric case and review of the literature. J Clin Neurosci 56:172–175PubMed
75.
Zurück zum Zitat Weetman RM, Rider PS, Oei TO et al (1976) Effect of diet on urinary excretion of VMA, HVA, metanephrine, and total free catecholamine in normal preschool children. J Pediatr 88:46–50PubMed Weetman RM, Rider PS, Oei TO et al (1976) Effect of diet on urinary excretion of VMA, HVA, metanephrine, and total free catecholamine in normal preschool children. J Pediatr 88:46–50PubMed
76.
Zurück zum Zitat Sundell IB, Hallmans G, Nilsson TK, Nygren C (1989) Plasma glucose and insulin, urinary catecholamine and cortisol responses to test breakfasts with high or low fibre content: the importance of the previous diet. Ann Nutr Metab 33:333–340PubMed Sundell IB, Hallmans G, Nilsson TK, Nygren C (1989) Plasma glucose and insulin, urinary catecholamine and cortisol responses to test breakfasts with high or low fibre content: the importance of the previous diet. Ann Nutr Metab 33:333–340PubMed
77.
Zurück zum Zitat Tormo C, Lumbreras B, Santos A et al (2009) Strategies for improving the collection of 24-hour urine for analysis in the clinical laboratory: redesigned instructions, opinion surveys, and application of reference change value to micturition. Arch Pathol Lab Med 133:1954–1960PubMed Tormo C, Lumbreras B, Santos A et al (2009) Strategies for improving the collection of 24-hour urine for analysis in the clinical laboratory: redesigned instructions, opinion surveys, and application of reference change value to micturition. Arch Pathol Lab Med 133:1954–1960PubMed
78.
Zurück zum Zitat Smith SJ, Diehl NN, Smith BD, Mohney BG (2010) Urine catecholamine levels as diagnostic markers for neuroblastoma in a defined population: implications for ophthalmic practice. Eye (Lond) 24:1792–1796 Smith SJ, Diehl NN, Smith BD, Mohney BG (2010) Urine catecholamine levels as diagnostic markers for neuroblastoma in a defined population: implications for ophthalmic practice. Eye (Lond) 24:1792–1796
79.
Zurück zum Zitat Park JR, Eggert A, Caron H (2010) Neuroblastoma: biology, prognosis, and treatment. Hematol Oncol Clin North Am 24:65–86PubMed Park JR, Eggert A, Caron H (2010) Neuroblastoma: biology, prognosis, and treatment. Hematol Oncol Clin North Am 24:65–86PubMed
80.
Zurück zum Zitat Laug WE, Siegel SE, Shaw KN et al (1978) Initial urinary catecholamine metabolite concentrations and prognosis in neuroblastoma. Pediatrics 62:77–83PubMed Laug WE, Siegel SE, Shaw KN et al (1978) Initial urinary catecholamine metabolite concentrations and prognosis in neuroblastoma. Pediatrics 62:77–83PubMed
81.
Zurück zum Zitat LaBrosse EH, Com-Nougue C, Zucker JM et al (1980) Urinary excretion of 3-methoxy-4-hydroxymandelic acid and 3-methoxy-4-hydroxyphenylacetic acid by 288 patients with neuroblastoma and related neural crest tumors. Cancer Res 40:1995–2001PubMed LaBrosse EH, Com-Nougue C, Zucker JM et al (1980) Urinary excretion of 3-methoxy-4-hydroxymandelic acid and 3-methoxy-4-hydroxyphenylacetic acid by 288 patients with neuroblastoma and related neural crest tumors. Cancer Res 40:1995–2001PubMed
82.
Zurück zum Zitat Park JR, Bagatell R, Cohn SL et al (2017) Revisions to the International Neuroblastoma Response Criteria: a consensus statement from the National Cancer Institute clinical trials planning meeting. J Clin Oncol 35:2580–2587 Park JR, Bagatell R, Cohn SL et al (2017) Revisions to the International Neuroblastoma Response Criteria: a consensus statement from the National Cancer Institute clinical trials planning meeting. J Clin Oncol 35:2580–2587
83.
Zurück zum Zitat El-Sayed AAF (2014) The prognostic value of concurrent Horner syndrome in extended Erb obstetric brachial plexus palsy. J Child Neurol 29:1356–1359PubMed El-Sayed AAF (2014) The prognostic value of concurrent Horner syndrome in extended Erb obstetric brachial plexus palsy. J Child Neurol 29:1356–1359PubMed
84.
Zurück zum Zitat Yoshida K, Kawabata H (2018) The prognostic value of concurrent Horner syndrome in surgical decision making at 3 months in total-type neonatal brachial plexus palsy. J Hand Surg Eur Vol 43:609–612PubMed Yoshida K, Kawabata H (2018) The prognostic value of concurrent Horner syndrome in surgical decision making at 3 months in total-type neonatal brachial plexus palsy. J Hand Surg Eur Vol 43:609–612PubMed
85.
Zurück zum Zitat Lequin MH, Peeters EAJ, Holscher HC et al (2004) Arterial infarction caused by carotid artery dissection in the neonate. Eur J Paediatr Neurol 8:155–160PubMed Lequin MH, Peeters EAJ, Holscher HC et al (2004) Arterial infarction caused by carotid artery dissection in the neonate. Eur J Paediatr Neurol 8:155–160PubMed
86.
Zurück zum Zitat Moore SW, Satge D, Sasco AJ et al (2003) The epidemiology of neonatal tumours. Report of an international working group. Pediatr Surg Int 19:509–519PubMed Moore SW, Satge D, Sasco AJ et al (2003) The epidemiology of neonatal tumours. Report of an international working group. Pediatr Surg Int 19:509–519PubMed
87.
Zurück zum Zitat Raciborska A, Bilska K, Weclawek-Tompol J et al (2016) Solid cancers in the premature and the newborn: report of three national referral centers. Pediatr Neonatol 57:295–301 Raciborska A, Bilska K, Weclawek-Tompol J et al (2016) Solid cancers in the premature and the newborn: report of three national referral centers. Pediatr Neonatol 57:295–301
88.
Zurück zum Zitat Desandes E, Guissou S, Ducassou S, Lacour B (2016) Neonatal solid tumors: incidence and survival in France. Pediatr Blood Cancer 63:1375–1380PubMed Desandes E, Guissou S, Ducassou S, Lacour B (2016) Neonatal solid tumors: incidence and survival in France. Pediatr Blood Cancer 63:1375–1380PubMed
89.
Zurück zum Zitat Chandrasekaran A (2018) Neonatal solid tumors. Pediatr Neonatol 59:65–70 Chandrasekaran A (2018) Neonatal solid tumors. Pediatr Neonatol 59:65–70
90.
Zurück zum Zitat Vo KT, Matthay KK, Neuhaus J et al (2014) Clinical, biologic, and prognostic differences on the basis of primary tumor site in neuroblastoma: a report from the international neuroblastoma risk group project. J Clin Oncol 32:3169–3176PubMedPubMedCentral Vo KT, Matthay KK, Neuhaus J et al (2014) Clinical, biologic, and prognostic differences on the basis of primary tumor site in neuroblastoma: a report from the international neuroblastoma risk group project. J Clin Oncol 32:3169–3176PubMedPubMedCentral
91.
92.
Zurück zum Zitat Jnah AJ, Evans SK, Sewell K, Trembath A (2019) Neuroblastoma in a neonate: a case report. Neonatal Netw 38:341–347PubMed Jnah AJ, Evans SK, Sewell K, Trembath A (2019) Neuroblastoma in a neonate: a case report. Neonatal Netw 38:341–347PubMed
93.
Zurück zum Zitat Dresler S, Harvey DG, Levisohn PM (1979) Retroperitoneal neuroblastoma widely metastatic to the central nervous system. Ann Neurol 5:196–198PubMed Dresler S, Harvey DG, Levisohn PM (1979) Retroperitoneal neuroblastoma widely metastatic to the central nervous system. Ann Neurol 5:196–198PubMed
94.
Zurück zum Zitat Lee SY, Chuang JH, Huang CB et al (1998) Congenital bilateral cystic neuroblastoma with liver metastases and massive intracystic haemorrhage. Br J Radiol 71:1205–1207PubMed Lee SY, Chuang JH, Huang CB et al (1998) Congenital bilateral cystic neuroblastoma with liver metastases and massive intracystic haemorrhage. Br J Radiol 71:1205–1207PubMed
95.
Zurück zum Zitat Sul HJ, Kang DY (2003) Congenital neuroblastoma with multiple metastases: a case report. J Korean Med Sci 18:618–620PubMedPubMedCentral Sul HJ, Kang DY (2003) Congenital neuroblastoma with multiple metastases: a case report. J Korean Med Sci 18:618–620PubMedPubMedCentral
96.
Zurück zum Zitat Schiavetti A, Foco M, Ingrosso A et al (2009) Congenital stage 1 neuroblastoma evolved into stage 4s. J Pediatr Hematol Oncol 31:59–60PubMed Schiavetti A, Foco M, Ingrosso A et al (2009) Congenital stage 1 neuroblastoma evolved into stage 4s. J Pediatr Hematol Oncol 31:59–60PubMed
97.
Zurück zum Zitat Tajiri T, Souzaki R, Kinoshita Y et al (2010) Concordance for neuroblastoma in monozygotic twins: case report and review of the literature. J Pediatr Surg 45:2312–2316PubMed Tajiri T, Souzaki R, Kinoshita Y et al (2010) Concordance for neuroblastoma in monozygotic twins: case report and review of the literature. J Pediatr Surg 45:2312–2316PubMed
98.
Zurück zum Zitat Wader JV, Kumbhar SS, Shukla DB, Mavi S (2015) Disseminated congenital neuroblastoma — an autopsy case report. J Clin Diagn Res 9:ED03–ED04PubMedPubMedCentral Wader JV, Kumbhar SS, Shukla DB, Mavi S (2015) Disseminated congenital neuroblastoma — an autopsy case report. J Clin Diagn Res 9:ED03–ED04PubMedPubMedCentral
99.
Zurück zum Zitat Starchenko II, Dyachenko LV, Prylutskyi OK et al (2019) The observation of congenital retroperitoneal large size neuroblastoma. Exp Oncol 41:179–181PubMed Starchenko II, Dyachenko LV, Prylutskyi OK et al (2019) The observation of congenital retroperitoneal large size neuroblastoma. Exp Oncol 41:179–181PubMed
100.
Zurück zum Zitat Claros P, Bandos R, Gilea I et al (1999) Major congenital anomalies of the internal carotid artery: agenesis, aplasia and hypoplasia. Int J Pediatr Otorhinolaryngol 49:69–76PubMed Claros P, Bandos R, Gilea I et al (1999) Major congenital anomalies of the internal carotid artery: agenesis, aplasia and hypoplasia. Int J Pediatr Otorhinolaryngol 49:69–76PubMed
101.
Zurück zum Zitat Farhat W, Ahdab R, Hosseini H (2011) Congenital agenesis of internal carotid artery with ipsilateral Horner presenting as focal neurological symptoms. Vasc Health Risk Manag 7:37–40PubMedPubMedCentral Farhat W, Ahdab R, Hosseini H (2011) Congenital agenesis of internal carotid artery with ipsilateral Horner presenting as focal neurological symptoms. Vasc Health Risk Manag 7:37–40PubMedPubMedCentral
102.
Zurück zum Zitat Hageman G, Ippel PF, te Nijenhuis FC (1992) Autosomal dominant congenital Horner's syndrome in a Dutch family. J Neurol Neurosurg Psychiatry 55:28–30PubMedPubMedCentral Hageman G, Ippel PF, te Nijenhuis FC (1992) Autosomal dominant congenital Horner's syndrome in a Dutch family. J Neurol Neurosurg Psychiatry 55:28–30PubMedPubMedCentral
103.
Zurück zum Zitat Graef S, Irwin MS, Wan MJ (2020) Incidence and prognostic role of the ocular manifestations of neuroblastoma in children. Am J Ophthalmol 213:145–152PubMed Graef S, Irwin MS, Wan MJ (2020) Incidence and prognostic role of the ocular manifestations of neuroblastoma in children. Am J Ophthalmol 213:145–152PubMed
104.
Zurück zum Zitat Cohen MD, Auringer ST, Grosfeld JL et al (1993) Multifocal primary neuroblastoma. Pediatr Radiol 23:463–466PubMed Cohen MD, Auringer ST, Grosfeld JL et al (1993) Multifocal primary neuroblastoma. Pediatr Radiol 23:463–466PubMed
105.
Zurück zum Zitat Williams P, Wegner E, Ziegler DS (2014) Outcomes in multifocal neuroblastoma as part of the neurocristopathy syndrome. Pediatrics 134:e611–e616PubMed Williams P, Wegner E, Ziegler DS (2014) Outcomes in multifocal neuroblastoma as part of the neurocristopathy syndrome. Pediatrics 134:e611–e616PubMed
Metadaten
Titel
Imaging of Horner syndrome in pediatrics: association with neuroblastoma
verfasst von
Hedieh Khalatbari
Gisele E. Ishak
Publikationsdatum
06.10.2020
Verlag
Springer Berlin Heidelberg
Erschienen in
Pediatric Radiology / Ausgabe 2/2021
Print ISSN: 0301-0449
Elektronische ISSN: 1432-1998
DOI
https://doi.org/10.1007/s00247-020-04796-w

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