Skip to main content
Erschienen in: Journal of Medical Case Reports 1/2019

Open Access 01.12.2019 | Case report

Parry–Romberg syndrome associated with en coup de sabre in a patient from South Sudan – a rare entity from East Africa: a case report

verfasst von: Jimmy Girgis William Abdelnour, Youeil Girgis William Abdelnour, Rose-Mery Amin Boushra Kerollos, Ziryab Imad Taha Mahmoud

Erschienen in: Journal of Medical Case Reports | Ausgabe 1/2019

Abstract

Background

Parry–Romberg syndrome, also known as progressive hemifacial atrophy, is a rare degenerative disorder with numerous distinctive clinical presentations. It is usually slowly progressive, occurring more in females, and affects primarily one side of the face; it causes unilateral atrophy and loss of skin, subcutaneous tissue, muscles, and bones, and can even extend to oral structures. Other involvements that can occur are ocular and neurological; however, it is frequently associated with linear scleroderma, known as en coup de sabre. The etiology of the disorder is unknown, although some consider it a variant of morphea (localized scleroderma) and others proposed a malfunction of the sympathetic system as a cause. Imaging studies can support diagnosis and reveal the extent of the disease. Moreover, with the wide systemic involvement in such a condition, a multidisciplinary approach is crucial.

Case presentation

A 35-year-old Dinka woman presented with left hemifacial atrophy associated with left-sided body hemihypoesthesia and glaucoma with overlapping linear scleroderma “en coup de sabre” for 5 years.

Conclusions

Parry–Romberg syndrome is a very rare entity causing progressive hemifacial atrophy that could also be associated with linear scleroderma. It has devastating outcomes due to its various systemic involvements; therefore, a multidisciplinary approach is required together with further studies to be performed in order to identify the key etiology and construct a clear guideline for management.
Abkürzungen
ANA
Antinuclear antibody
B-scan
Brightness scan
CCP
Cyclic citrullinated peptides
CT
Computed tomographyEEG
Electroencephalogram
IOP
Intraocular pressure
OPG
Orthopantomogram
PRS
Parry–Romberg syndrome
VA
Visual acuity

Background

Parry–Romberg syndrome (PRS), also known as progressive hemifacial atrophy, was originally described by Caleb Hillier Parry in 1815, then it was described with further details by Moritz Heinrich Romberg in 1846 and in 1871 Eulenberg established the term “progressive facial hemiatrophy” [13]. It is a developmental craniofacial disorder of unknown etiology characterized by a slowly progressive unilateral facial atrophy and is associated with different systemic manifestations. In particular, it is associated with maxillofacial manifestations (wasting of masticatory muscles, delayed ipsilateral tooth eruption, unilateral tongue atrophy, jaw hypoplasia), and neurological (trigeminal neuralgia, migraine, seizures) and ophthalmologic abnormalities (enophthalmos, glaucoma, endothelial precipitates, Horner’s syndrome, ophthalmoplegia) [49]. Moreover, it is frequently associated with linear scleroderma and referred to as en coup de sabre [10, 11].
Onset of the disease is in childhood, typically during the first two decades of life, although later onset has previously been described. Usually, the atrophy progresses slowly for several years and afterward it becomes stable with females being affected more than males [11, 12].
Almost two centuries after this disease was defined, the etiology has still not been determined. Autoimmune disease and other causes like metabolic disorders and trauma have been postulated; sometimes, familial cases with autosomal dominant inheritance have been seen.
Concerning the treatment, there is no cure although reconstructive surgery with immunosuppressive drugs have been used and showed considerable results [10, 13].
What is unusual about the present case is the rather late onset at age of 30, the static type of progression, and the hemihypoesthesia.

Case presentation

A 35-year-old Dinka woman from South Sudan presented with left-sided facial asymmetry associated with numbness on the left side of her body and deteriorating vision in her left eye. Her symptoms started 5 years earlier with slowly progressive left-sided facial atrophy associated with reduced vision in her left eye and early morning blurred vision. Two years later she started feeling numbness on the left side of her body (upper limb and lower limb spontaneously). Numbness and atrophy became static in the last year with further deterioration in vision.
She never had any seizures or history of a psychiatric illness. There was no family history of a similar condition; she was not on any medication or known to have any chronic illness.
On examination, there was noticeable left-sided facial atrophy extending from the frontal bone to mental region associated with enophthalmos affecting her left eye, minimal tongue atrophy on the same side, and clear coup de sabre in her left cheek (Fig. 1). An intraoral examination revealed minimal tongue atrophy on the left side, badly decayed right maxillary third molar together with the mandibular second and third molars, and there were caries on left mandibular and maxillary third molars.
Her cranial nerves were intact, however, there was decreased sensation (fine touch and pin prick) affecting the left side of her body (including the left side of her face), although tone, reflexes, and proprioception were all intact. An examination of her right side was unremarkable. An ophthalmic examination showed a left eye visual acuity (VA) of 6/40, keratic precipitates, immature cataract, raised intraocular pressure (IOP) of 26, and hazy fundoscopy; however, she had a normal right eye with VA of 6/6 and IOP of 12.2. A brightness scan (B-scan) was performed and it was normal in both eyes (Fig. 2). Other systemic examinations of her heart, chest, and abdomen were unremarkable.
A diagnosis of PRS with overlapped linear scleroderma was postulated and further radiologic and laboratory assessments were made.
General routine investigations revealed normocytic normochromic anemia probably due to amoebiasis infection found in her stool sample (no other agents were seen such as ova or worms) which was corrected after treatment. Liver and renal function tests were within normal ranges as was her vitamin B12 level. Furthermore, rheumatoid factor was positive yet antinuclear antibody (ANA) profile and anti-cyclic citrullinated peptide (CCP) tests were all negative. Laboratory results are shown in Table 1.
Table 1
Lab Test Results
Laboratory Results
CBC
Hb
10.6
ESR
10 mm/hour
PCV
32.1
Vitamin B12
412 pg/mL (221–950)
RBCs
3.99
Rh. factor
> 8 IU/mL Positive
MCV
80.5
Anti-CCP
9.7 AU/mL
Negative
MCH
26.6
   
MCHC
33
 
SM
Negative
TWBCs
3900
 
SS-A
Negative
N
54%
 
Ro52
Negative
L
37%
 
SS-B
Negative
M
8%
 
ScL 70
Negative
E
1%
ANA profile
JO-1
Negative
PLT
265,000
 
DsDNA
Negative
RFT
Urea
24
 
Nucleosomes
Negative
Creatinine
0.7
 
Histones
Negative
Na +
132
 
Rib p-protein
Negative
K +
3.6
 
AMA M2
Negative
Ca 2+
9.9
 
PCNA
Negative
PO 3+
3.4
 
PM-SCL
Negative
LFT
T. protein
7.3
 
CENPB
Negative
 
Nrnp/SM
Negative
S. albumin
4.5
   
Globulin
2.8
   
T. bilirubin
0.52
   
D. bilirubin
0.3
   
I. bilirubin
0.22
   
ALT
16
   
AST
20
   
ALP
72
   
ALP alkaline phosphatase, ALT alanine aminotransferase, AMA M2 anti-mitochondrial M2 antibody, AST aspartate aminotransferase, ANA antinuclear antibody, CBC complete blood count, CCP cyclic citrullinated peptide, CENPB centromere protein B, D. direct, Ds double-stranded, E erythrocyte, ESR erythrocyte sedimentation rate, Hb hemoglobin, I. indirect, L leukocyte, LFT liver function test, M monocyte, MCH mean corpuscular hemoglobin, MCHC mean corpuscular hemoglobin concentration, MCV mean corpuscular volume, N neutrophil, PCNA proliferating cell nuclear antigen, PCV packed cell volume, PLT platelet, PM-SCL polymyositis/scleroderma (exosome) autoantigen, RBC red blood cells, RFT renal function test, Rh. rhesus, Rib ribosomal, S. serum, SS-A Sjögren syndrome antigen A or Ro, SS-B Sjögren syndrome antigen B or La, T. total, TWBC total white blood cell
Radiological imaging with computed tomography (CT) scan of her facial bones revealed mild asymmetry of her face with early affection of the left zygomatic bone. There was obvious atrophy involving left-sided facial subcutaneous tissue extending to the masseter muscle (Fig. 2). Moreover, an orthopantomogram (OPG) showed multilocular radiolucency at the left angle of her mandible with remaining roots in the left mandibular third molar, decay in the maxillary left third molar (appeared as radiolucency in the enamel and dentine occlusally), an unerupted right maxillary third molar, and badly decayed mandibular third molar teeth (Fig. 3).
An electroencephalogram (EEG) revealed normal study: normal 9 Hz, α-rhythm in awake EEG with no epileptiform activity seen.
Two skin biopsies were requested that reported: skin with hyperkeratosis, follicular plugging, thin stratum Malpighii, and focal vacuolar degeneration of the basal layer with presence of dermal thick collagen fibers and mononuclear inflammatory cellular infiltration. This picture was consistent with linear scleroderma overlapping PRS.

Discussion

PRS is a rare neurocutaneous disorder of unknown origin. It is characterized by slowly progressive facial hemiatrophy affecting all tissue layers from skin to bone and frequently (21–31%) overlaps with a condition known as linear scleroderma “en coup de sabre.” It has a prevalence rate of 1 in 70,000 with no difference in rates between different ethnic groups. However, only four cases were reported from Africa in the English language literature: Gueye A, et al. [14], Singh M, et al. [15], Ilhame N, et al. [16], and Elsaid N, et al. [17] from Senegal, Libya, Morocco, and Egypt, respectively. It affects mainly females and usually involves the left side of the face. In most patients (71%), disease onset commences before the age of 15 years and only 8% had an onset after the age of 25 years, as was the case in our patient. Earlier onset and longer duration of PRS have been reported to relate to increased severity of the disease [11, 12, 1820]
A cerebral disturbance of fat metabolism and atrophic malformation of cervical sympathetic nervous system have been proposed as the primary cause. Other possible factors that are involved in the pathogenesis include trauma, infections (Borrelia burgdorferi and viral), heredity, endocrine disturbances, and autoimmunity [21, 22].
It is associated with different systemic manifestations. It commonly affects the dermatomes of one or multiple branches of the trigeminal nerve with atrophy of the skin and underlying structures (soft tissues, muscles, and bones) and can also affect the eye (enophthalmos, uveitis, retinal vasculitis, glaucoma, central retinal artery occlusion, heterochromic iridocyclitis, restrictive strabismus, Coats disease, papillitis, optic atrophy, and neuroretinitis), the pupil (Horner syndrome, pupillary abnormalities), and hair (band-like alopecia). Also, various oral involvements have been described (unilateral tongue atrophy, jaw hypoplasia, wasting of the muscles of mastication, short roots on affected side, deficiency of soft and hard palate, delayed ipsilateral tooth eruption, and unilateral crossbite). The most commonly seen neurological involvements are epilepsy (60.5%) followed by pain (44.2%); moreover, cerebral vascular malformations have been seen (11.5%) [4, 12].
Multiple treatment modalities have been mentioned in the literature including:
I.
Medical
 
Corticosteroids (topical and intralesional), antioxidants, immunosuppressant (methotrexate), and retinoids.
II.
Surgical
 
Fascia grafts, muscle grafts, pedicle flaps, microvascular free flaps, and free fat grafts – injection of aspirated fat and alloplastic graft materials. Some surgical modalities classify the depression type caused by the disease and afterward select the surgical technique to be used [2224].

Conclusion

PRS is a very rare entity causing progressive hemifacial atrophy that could also be associated with linear scleroderma.
It has devastating outcomes due to its various systemic involvements; therefore, a multidisciplinary approach is required together with further studies to be performed in order to identify the key etiology and construct a clear guideline for management.

Acknowledgements

Dr Antony William was consulted for the ophthalmic findings in the case. Dr Vebronia Barsoum was consulted for the dental findings in the case.

Funding

None declared.

Availability of data and materials

The authors declare that all the data supporting the findings of this study are available within the article.

Authors’ information

Dr Jimmy Girgis William Abdelnour
MBBS, FCCS, MRCP (UK - Part 1), PGCert. DM (Queen Margaret University – Edinburgh).
Dr Youeil Girgis William Abdelnour
MBBS, MSc Pediatric Emergency (University of Edinburgh).
Dr Rose-Mery Amin Boushra Kerollos
MBBS.
Dr Ziryab Imad Taha Mahmoud
Consultant of Internal Medicine at Haj El-Safi Teaching Hospital,
Assistant Professor of Medicine and Head of Department of Internal Medicine at University of Bahri,
MBBS, MRCP (UK), MSc Clinical Pharmacology, Diploma of Research Methodology and Ethics, Rheumatology Fellowship trainee (SMSB).
Not applicable.
Written informed consent was obtained from the patient for publication of this case report and accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://​creativecommons.​org/​licenses/​by/​4.​0/​), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://​creativecommons.​org/​publicdomain/​zero/​1.​0/​) applies to the data made available in this article, unless otherwise stated.

Unsere Produktempfehlungen

e.Med Interdisziplinär

Kombi-Abonnement

Für Ihren Erfolg in Klinik und Praxis - Die beste Hilfe in Ihrem Arbeitsalltag

Mit e.Med Interdisziplinär erhalten Sie Zugang zu allen CME-Fortbildungen und Fachzeitschriften auf SpringerMedizin.de.

© Springer Medizin

Bis 11. April 2024 bestellen und im ersten Jahr 50 % sparen!

e.Med Allgemeinmedizin

Kombi-Abonnement

Mit e.Med Allgemeinmedizin erhalten Sie Zugang zu allen CME-Fortbildungen und Premium-Inhalten der allgemeinmedizinischen Zeitschriften, inklusive einer gedruckten Allgemeinmedizin-Zeitschrift Ihrer Wahl.

© Springer Medizin

Bis 11. April 2024 bestellen und im ersten Jahr 50 % sparen!

Literatur
1.
Zurück zum Zitat Parry CH. Collections from the Unpublished Medical Writings of the Late Caleb Hillier Parry. London: Underwoods; 1825. p. 478–80. Parry CH. Collections from the Unpublished Medical Writings of the Late Caleb Hillier Parry. London: Underwoods; 1825. p. 478–80.
2.
Zurück zum Zitat Romberg HM. Krankheiten des nervensystems (IV: Trophoneurosen). Klinische Ergebnisse. Berlin: Forrtner; 1846. p. 75–81. Romberg HM. Krankheiten des nervensystems (IV: Trophoneurosen). Klinische Ergebnisse. Berlin: Forrtner; 1846. p. 75–81.
3.
Zurück zum Zitat Kumar AA, Kumar RA, Shantha GPS, Aloogopinathan G. Progressive hemi facial atrophy – Parry Romberg syndrome presenting as severe facial pain in a young man: a case report. Cases J. 2009;2:6776.CrossRefPubMedPubMedCentral Kumar AA, Kumar RA, Shantha GPS, Aloogopinathan G. Progressive hemi facial atrophy – Parry Romberg syndrome presenting as severe facial pain in a young man: a case report. Cases J. 2009;2:6776.CrossRefPubMedPubMedCentral
4.
Zurück zum Zitat Al-Aizari NA, Azzeghaiby SN, Al-Shamiri HM, Darwish S, Tarakji B. Oral manifestations of Parry–Romberg syndrome: A review of literature. Avicenna J Med. 2015;5(2):25–8.CrossRefPubMedPubMedCentral Al-Aizari NA, Azzeghaiby SN, Al-Shamiri HM, Darwish S, Tarakji B. Oral manifestations of Parry–Romberg syndrome: A review of literature. Avicenna J Med. 2015;5(2):25–8.CrossRefPubMedPubMedCentral
5.
Zurück zum Zitat Tang XJ, Liu W, Yang B, Shi L, Yin L, Zhang ZY. Parry-Romberg syndrome with rare maxillofacial deformities: A report on two cases. J Craniomaxillofac Surg. 2014;42:780–3.CrossRefPubMed Tang XJ, Liu W, Yang B, Shi L, Yin L, Zhang ZY. Parry-Romberg syndrome with rare maxillofacial deformities: A report on two cases. J Craniomaxillofac Surg. 2014;42:780–3.CrossRefPubMed
6.
Zurück zum Zitat Pensler JM, Murphy GF, Mulliken JB. Clinical and ultrastructural studies of Romberg’s hemifacial atrophy. Plast Reconstr Surg. 1990;85:669–74.CrossRefPubMed Pensler JM, Murphy GF, Mulliken JB. Clinical and ultrastructural studies of Romberg’s hemifacial atrophy. Plast Reconstr Surg. 1990;85:669–74.CrossRefPubMed
7.
Zurück zum Zitat Ibarra PC. Parry-Romberg syndrome with glaucoma and pregnancy. Gac Med Mex. 2001;137:289. Ibarra PC. Parry-Romberg syndrome with glaucoma and pregnancy. Gac Med Mex. 2001;137:289.
8.
Zurück zum Zitat Banks TL, Sugar HS. Ocular manifestations of facial hemiatrophy. J Mt Sinai Hosp N Y. 1963;11:83. Banks TL, Sugar HS. Ocular manifestations of facial hemiatrophy. J Mt Sinai Hosp N Y. 1963;11:83.
9.
Zurück zum Zitat El KJ, Abbas O, Rubeiz M. A review of Parry Romberg syndrome. J Dermatol. 2012;67:769–84. El KJ, Abbas O, Rubeiz M. A review of Parry Romberg syndrome. J Dermatol. 2012;67:769–84.
10.
Zurück zum Zitat Millichap JGA. Neurological Syndromes. New York: Springer; 2013. p. 180.CrossRef Millichap JGA. Neurological Syndromes. New York: Springer; 2013. p. 180.CrossRef
11.
12.
Zurück zum Zitat Stone J. Parry-Romberg syndrome: a global survey of 205 patients using the Internet. Neurology. 2003;61:674–6.CrossRefPubMed Stone J. Parry-Romberg syndrome: a global survey of 205 patients using the Internet. Neurology. 2003;61:674–6.CrossRefPubMed
13.
Zurück zum Zitat Badam RK, Dara BB, Pallerla SR, Boringi M. Parry Romberg syndrome: A rare case report. J Indian Acad Oral Med Radiol. 2014;26:237–40.CrossRef Badam RK, Dara BB, Pallerla SR, Boringi M. Parry Romberg syndrome: A rare case report. J Indian Acad Oral Med Radiol. 2014;26:237–40.CrossRef
14.
Zurück zum Zitat Gueye A, Autret A. First case of facial hemiatrophy (Romberg's disease) observed in Senegal. Bull Soc Med Afr Noire Lang Fr. 1978;23(4):389–91.PubMed Gueye A, Autret A. First case of facial hemiatrophy (Romberg's disease) observed in Senegal. Bull Soc Med Afr Noire Lang Fr. 1978;23(4):389–91.PubMed
15.
Zurück zum Zitat Singh M, Bharija SC, Belhaj MS, Mangoush E. A: Romberg’s Syndrome: A Case Report. Dermatology. 1985;170:145–6.CrossRef Singh M, Bharija SC, Belhaj MS, Mangoush E. A: Romberg’s Syndrome: A Case Report. Dermatology. 1985;170:145–6.CrossRef
16.
Zurück zum Zitat Ilhame N, Christelle E, Mariam M, Karima S, Badredine H. Extra-Cephalic Involvement in the Syndrome of Parry Romberg. Clin Med Img Lib. 2017;3(3):1–3.CrossRef Ilhame N, Christelle E, Mariam M, Karima S, Badredine H. Extra-Cephalic Involvement in the Syndrome of Parry Romberg. Clin Med Img Lib. 2017;3(3):1–3.CrossRef
17.
Zurück zum Zitat Elsaid N, Saied A, El-Salam MA. Egyptian Case of Parry-Romberg Syndrome. American J Rare Dis Diagn Ther. 2018;1(1):001–3. Elsaid N, Saied A, El-Salam MA. Egyptian Case of Parry-Romberg Syndrome. American J Rare Dis Diagn Ther. 2018;1(1):001–3.
18.
Zurück zum Zitat Kumar S, Kumar D, Kumar R, Rajkumar, Prabhakar R. Parry-Romberg Syndrome: A Case of Late Onset with Rapid Progression. J Clin Diagn Res. 2014;8(9):ZD27–8.PubMedPubMedCentral Kumar S, Kumar D, Kumar R, Rajkumar, Prabhakar R. Parry-Romberg Syndrome: A Case of Late Onset with Rapid Progression. J Clin Diagn Res. 2014;8(9):ZD27–8.PubMedPubMedCentral
19.
Zurück zum Zitat Sharma M, Bharatha A, Antonyshyn OM, et al. Case 178: Parry-Romberg syndrome. Radiology. 2012;262:721–5.CrossRefPubMed Sharma M, Bharatha A, Antonyshyn OM, et al. Case 178: Parry-Romberg syndrome. Radiology. 2012;262:721–5.CrossRefPubMed
20.
Zurück zum Zitat Pichiecchio A, Uggetti C, Egitto MG, et al. Parry-Romberg syndrome with migraine and intracranial aneurysm. Neurology. 2002;59:606–8.CrossRefPubMed Pichiecchio A, Uggetti C, Egitto MG, et al. Parry-Romberg syndrome with migraine and intracranial aneurysm. Neurology. 2002;59:606–8.CrossRefPubMed
21.
Zurück zum Zitat Maletic J, Tsirka V, Ioannides P, Karacostas D, Taskos N. Parry-Romberg Syndrome Associated with Localized Scleroderma. Case Rep Neurol. 2010;2:57–62.CrossRefPubMedPubMedCentral Maletic J, Tsirka V, Ioannides P, Karacostas D, Taskos N. Parry-Romberg Syndrome Associated with Localized Scleroderma. Case Rep Neurol. 2010;2:57–62.CrossRefPubMedPubMedCentral
22.
Zurück zum Zitat Sargunar B, Ebenezer V, Balakrishnan R, Priya S. Parry Romberg Syndrome – A Review of Treatment Options. Biomed Pharmacol J. 2014;7(1).CrossRef Sargunar B, Ebenezer V, Balakrishnan R, Priya S. Parry Romberg Syndrome – A Review of Treatment Options. Biomed Pharmacol J. 2014;7(1).CrossRef
23.
Zurück zum Zitat Guerrerosantos J, Guerrerosantos F, Orozco J. Classification and treatment of facial tissue atrophy in Parry-Romberg disease. Aesth Plast Surg. 2007;31:424–34.CrossRef Guerrerosantos J, Guerrerosantos F, Orozco J. Classification and treatment of facial tissue atrophy in Parry-Romberg disease. Aesth Plast Surg. 2007;31:424–34.CrossRef
24.
Zurück zum Zitat Anderson LE, Treat JR, Licht DJ, Kreiger PA, Knight AM. Remission of seizures with immunosuppressive therapy in Parry-Romberg syndrome and en coup de sabre linear scleroderma: Case report and brief review of the literature. Pediatr Dermatol. 2018;35:e363–5.CrossRefPubMed Anderson LE, Treat JR, Licht DJ, Kreiger PA, Knight AM. Remission of seizures with immunosuppressive therapy in Parry-Romberg syndrome and en coup de sabre linear scleroderma: Case report and brief review of the literature. Pediatr Dermatol. 2018;35:e363–5.CrossRefPubMed
Metadaten
Titel
Parry–Romberg syndrome associated with en coup de sabre in a patient from South Sudan – a rare entity from East Africa: a case report
verfasst von
Jimmy Girgis William Abdelnour
Youeil Girgis William Abdelnour
Rose-Mery Amin Boushra Kerollos
Ziryab Imad Taha Mahmoud
Publikationsdatum
01.12.2019
Verlag
BioMed Central
Erschienen in
Journal of Medical Case Reports / Ausgabe 1/2019
Elektronische ISSN: 1752-1947
DOI
https://doi.org/10.1186/s13256-019-2063-2

Weitere Artikel der Ausgabe 1/2019

Journal of Medical Case Reports 1/2019 Zur Ausgabe