Skip to main content
Erschienen in: Neuroradiology 8/2018

17.06.2018 | Paediatric Neuroradiology

Rhinencephalon changes in tuberous sclerosis complex

verfasst von: Renzo Manara, Davide Brotto, Samuela Bugin, Maria Federica Pelizza, Stefano Sartori, Margherita Nosadini, Sara Azzolini, Giorgio Iaconetta, Cecilia Parazzini, Alessandra Murgia, Angela Peron, Paola Canevini, Francesca Labriola, Aglaia Vignoli, Irene Toldo

Erschienen in: Neuroradiology | Ausgabe 8/2018

Einloggen, um Zugang zu erhalten

Abstract

Purpose

Despite complex olfactory bulb embryogenesis, its development abnormalities in tuberous sclerosis complex (TSC) have been poorly investigated.

Methods

Brain MRIs of 110 TSC patients (mean age 11.5 years; age range 0.5–38 years; 52 female; 26 TSC1, 68 TSC2, 8 without mutation identified in TSC1 or TSC2, 8 not tested) were retrospectively evaluated. Signal and morphological abnormalities consistent with olfactory bulb hypo/aplasia or with olfactory bulb hamartomas were recorded. Cortical tuber number was visually assessed and a neurological severity score was obtained. Patients with and without rhinencephalon abnormalities were compared using appropriate parametric and non-parametric tests.

Results

Eight of110 (7.2%) TSC patients presented rhinencephalon MRI changes encompassing olfactory bulb bilateral aplasia (2/110), bilateral hypoplasia (2/110), unilateral hypoplasia (1/110), unilateral hamartoma (2/110), and bilateral hamartomas (1/110); olfactory bulb hypo/aplasia always displayed ipsilateral olfactory sulcus hypoplasia, while no TSC patient harboring rhinencephalon hamartomas had concomitant forebrain sulcation abnormalities. None of the patients showed overt olfactory deficits or hypogonadism, though young age and poor compliance hampered a proper evaluation in most cases. TSC patients with rhinencephalon changes had more cortical tubers (47 ± 29.1 vs 26.2 ± 19.6; p = 0.006) but did not differ for clinical severity (p = 0.45) compared to the other patients of the sample.

Conclusions

Olfactory bulb and/or forebrain changes are not rare among TSC subjects. Future studies investigating clinical consequences in older subjects (anosmia, gonadic development etc.) will define whether rhinencephalon changes are simply an imaging feature among the constellation of TSC-related brain changes or a feature to be searched for possible implications in the management of TSC subjects.
Anhänge
Nur mit Berechtigung zugänglich
Literatur
1.
2.
Zurück zum Zitat Curatolo P, Moavero R, de Vries PJ (2015) Neurological and neuropsychiatric aspects of tuberous sclerosis complex. Lancet Neurol 14:733–745CrossRefPubMed Curatolo P, Moavero R, de Vries PJ (2015) Neurological and neuropsychiatric aspects of tuberous sclerosis complex. Lancet Neurol 14:733–745CrossRefPubMed
3.
Zurück zum Zitat Northrup H, Krueger DA, on behalf of the International Tuberous Sclerosis Complex Consensus Group: Tuberous Sclerosis Complex Diagnostic Criteria Update (2013) Recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference. Pediatr Neurol 49:243–254CrossRefPubMedPubMedCentral Northrup H, Krueger DA, on behalf of the International Tuberous Sclerosis Complex Consensus Group: Tuberous Sclerosis Complex Diagnostic Criteria Update (2013) Recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference. Pediatr Neurol 49:243–254CrossRefPubMedPubMedCentral
4.
Zurück zum Zitat Kingswood C, Bolton P, Crawford P, Harland C, Johnson SR, Sampson JR, Shepherd C, Spink J, Demuth D, Lucchese L, Nasuti P, Gray E, Pinnegar A, Magestro M (2016) The clinical profile of tuberous sclerosis complex (TSC) in the United Kingdom: a retrospective cohort study in the Clinical Practice Research Datalink (CPRD). Eur J Paediatr Neurol 20(2):296–308CrossRefPubMed Kingswood C, Bolton P, Crawford P, Harland C, Johnson SR, Sampson JR, Shepherd C, Spink J, Demuth D, Lucchese L, Nasuti P, Gray E, Pinnegar A, Magestro M (2016) The clinical profile of tuberous sclerosis complex (TSC) in the United Kingdom: a retrospective cohort study in the Clinical Practice Research Datalink (CPRD). Eur J Paediatr Neurol 20(2):296–308CrossRefPubMed
5.
Zurück zum Zitat Boer K, Troost D, Jansen F, Nellist M, van den Ouweland AM, Geurts JJ, Spliet WG, Crino P, Aronica E (2008) Clinicopathological and immunohistochemical findings in an autopsy case of tuberous sclerosis complex. Neuropathology 28(6):577–590PubMed Boer K, Troost D, Jansen F, Nellist M, van den Ouweland AM, Geurts JJ, Spliet WG, Crino P, Aronica E (2008) Clinicopathological and immunohistochemical findings in an autopsy case of tuberous sclerosis complex. Neuropathology 28(6):577–590PubMed
6.
Zurück zum Zitat Boronat S, Shaaya EA, Auladell M, Thiele EA, Caruso P (2014) Intracranial arteriopathy in tuberous sclerosis complex. J Child Neurol 29:912–919CrossRefPubMed Boronat S, Shaaya EA, Auladell M, Thiele EA, Caruso P (2014) Intracranial arteriopathy in tuberous sclerosis complex. J Child Neurol 29:912–919CrossRefPubMed
7.
Zurück zum Zitat Tortori-Donati P, Rossi A (2005) Pediatric neuroradiology brain. Springer-Verlag, Berlin, pp 785–800CrossRef Tortori-Donati P, Rossi A (2005) Pediatric neuroradiology brain. Springer-Verlag, Berlin, pp 785–800CrossRef
8.
Zurück zum Zitat Sarnat HB, Flores-Sarnat L (2017) Olfactory development, part 2: neuroanatomic maturation and dysgeneses. J Child Neurol 32(6):579–593CrossRefPubMed Sarnat HB, Flores-Sarnat L (2017) Olfactory development, part 2: neuroanatomic maturation and dysgeneses. J Child Neurol 32(6):579–593CrossRefPubMed
9.
Zurück zum Zitat Manara R, Salvalaggio A, Favaro A, Palumbo V, Citton V, Elefante A, Brunetti A, Di Salle F, Bonanni G, Sinisi AA (2014) Kallmann syndrome neuroradiological study group. Brain changes in Kallmann syndrome. AJNR Am J Neuroradiol 35(9):1700–1706CrossRefPubMed Manara R, Salvalaggio A, Favaro A, Palumbo V, Citton V, Elefante A, Brunetti A, Di Salle F, Bonanni G, Sinisi AA (2014) Kallmann syndrome neuroradiological study group. Brain changes in Kallmann syndrome. AJNR Am J Neuroradiol 35(9):1700–1706CrossRefPubMed
10.
Zurück zum Zitat Quinton R, Duke VM, de Zoysa PA, Platts AD, Valentine A, Kendall B, Pickman S, Kirk JM, Besser GM, Jacobs HS, Bouloux PM (1996) The neuroradiology of Kallmann’s syndrome: a genotypic and phenotypic analysis. J Clin Endocrinol Metab 81(8):3010–3017PubMed Quinton R, Duke VM, de Zoysa PA, Platts AD, Valentine A, Kendall B, Pickman S, Kirk JM, Besser GM, Jacobs HS, Bouloux PM (1996) The neuroradiology of Kallmann’s syndrome: a genotypic and phenotypic analysis. J Clin Endocrinol Metab 81(8):3010–3017PubMed
11.
Zurück zum Zitat de León GA, Zaeri N, Foley CM (1988) Olfactory hamartomas in tuberous sclerosis. J Neurol Sci 87(2–3):187–194CrossRefPubMed de León GA, Zaeri N, Foley CM (1988) Olfactory hamartomas in tuberous sclerosis. J Neurol Sci 87(2–3):187–194CrossRefPubMed
12.
Zurück zum Zitat Feliciano DM, Quon JL, Su T, Taylor MM, Bordey A (2012) Postnatal neurogenesis generates heterotopias, olfactory micronodules and cortical infiltration following single-cell Tsc1 deletion. Hum Mol Genet 21(4):799–810CrossRefPubMed Feliciano DM, Quon JL, Su T, Taylor MM, Bordey A (2012) Postnatal neurogenesis generates heterotopias, olfactory micronodules and cortical infiltration following single-cell Tsc1 deletion. Hum Mol Genet 21(4):799–810CrossRefPubMed
13.
Zurück zum Zitat Wong AM, Wang HS, Schwartz ES, Toh CH, Zimmerman RA, Liu PL, Wu YM, Ng SH, Wang JJ (2013) Cerebral diffusion tensor MR tractography in tuberous sclerosis complex: correlation with neurologic severity and tract-based spatial statistical analysis. AJNR Am J Neuroradiol 34:1829–1835CrossRefPubMed Wong AM, Wang HS, Schwartz ES, Toh CH, Zimmerman RA, Liu PL, Wu YM, Ng SH, Wang JJ (2013) Cerebral diffusion tensor MR tractography in tuberous sclerosis complex: correlation with neurologic severity and tract-based spatial statistical analysis. AJNR Am J Neuroradiol 34:1829–1835CrossRefPubMed
14.
Zurück zum Zitat Ottaviano G, Cantone E, D'Errico A, Salvalaggio A, Citton V, Scarpa B, Favaro A, Sinisi AA, Liuzzi R, Bonanni G, Di Salle F, Elefante A, Manara R, Staffieri A, Martini A, Brunetti A (2015) Sniffin’ Sticks and olfactory system imaging in patients with Kallmann syndrome. Int Forum Allergy Rhinol 5(9):855–861CrossRefPubMed Ottaviano G, Cantone E, D'Errico A, Salvalaggio A, Citton V, Scarpa B, Favaro A, Sinisi AA, Liuzzi R, Bonanni G, Di Salle F, Elefante A, Manara R, Staffieri A, Martini A, Brunetti A (2015) Sniffin’ Sticks and olfactory system imaging in patients with Kallmann syndrome. Int Forum Allergy Rhinol 5(9):855–861CrossRefPubMed
15.
Zurück zum Zitat Cabrera SM, Rogol AD (2013) Testosterone exposure in childhood: discerning pathology from physiology. Expert Opin Drug Saf 12(3):375–388CrossRefPubMed Cabrera SM, Rogol AD (2013) Testosterone exposure in childhood: discerning pathology from physiology. Expert Opin Drug Saf 12(3):375–388CrossRefPubMed
16.
Zurück zum Zitat Manara R, Bugin S, Pelizza MF, Sartori S, Nosadini M, Labriola F, Canevini P, Vignoli A, Toldo I (2018) Genetic and imaging features of cerebellar abnormalities in tuberous sclerosis complex: more insights into their pathogenesis. Dev Med Child Neurol 60(7):724-725 Manara R, Bugin S, Pelizza MF, Sartori S, Nosadini M, Labriola F, Canevini P, Vignoli A, Toldo I (2018) Genetic and imaging features of cerebellar abnormalities in tuberous sclerosis complex: more insights into their pathogenesis. Dev Med Child Neurol 60(7):724-725
17.
Zurück zum Zitat Boronat S, Thiele EA, Caruso P (2017) Cerebellar lesions are associated with TSC2 mutations in tuberous sclerosis complex: a retrospective record review study. Dev Med Child Neurol 59(10):1071–1076CrossRefPubMed Boronat S, Thiele EA, Caruso P (2017) Cerebellar lesions are associated with TSC2 mutations in tuberous sclerosis complex: a retrospective record review study. Dev Med Child Neurol 59(10):1071–1076CrossRefPubMed
18.
Zurück zum Zitat Au KS, Williams AT, Roach ES, Batchelor L, Sparagana SP, Delgado MR, Wheless JW, Baumgartner JE, Roa BB, Wilson CM, Smith-Knuppel TK, Cheung MY, Whittemore VH, King TM, Northrup H (2007) Genotype/phenotype correlation in 325 individuals referred for a diagnosis of tuberous sclerosis complex in the United States. Genet Med 9:88–100CrossRefPubMed Au KS, Williams AT, Roach ES, Batchelor L, Sparagana SP, Delgado MR, Wheless JW, Baumgartner JE, Roa BB, Wilson CM, Smith-Knuppel TK, Cheung MY, Whittemore VH, King TM, Northrup H (2007) Genotype/phenotype correlation in 325 individuals referred for a diagnosis of tuberous sclerosis complex in the United States. Genet Med 9:88–100CrossRefPubMed
Metadaten
Titel
Rhinencephalon changes in tuberous sclerosis complex
verfasst von
Renzo Manara
Davide Brotto
Samuela Bugin
Maria Federica Pelizza
Stefano Sartori
Margherita Nosadini
Sara Azzolini
Giorgio Iaconetta
Cecilia Parazzini
Alessandra Murgia
Angela Peron
Paola Canevini
Francesca Labriola
Aglaia Vignoli
Irene Toldo
Publikationsdatum
17.06.2018
Verlag
Springer Berlin Heidelberg
Erschienen in
Neuroradiology / Ausgabe 8/2018
Print ISSN: 0028-3940
Elektronische ISSN: 1432-1920
DOI
https://doi.org/10.1007/s00234-018-2045-x

Weitere Artikel der Ausgabe 8/2018

Neuroradiology 8/2018 Zur Ausgabe

Leitlinien kompakt für die Neurologie

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

Update Neurologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.