RARE ORAL FINDINGS OF A PEDIATRIC PATIENT WITH PARRY ROMBERG SYNDROME: A CASE REPORT
Year 2024,
Volume: 13 Issue: 1, 155 - 160, 26.01.2024
Derya Sarıoğlu
,
Özge Anıl
Abstract
Scleroderma is a chronic disease that causes thickening and hardening of the skin and subcutaneous tissues, resulting from disorders in collagen production and destruction. The most common type of scleroderma in children, which has many subtypes; is the linear form of localized scleroderma, in other words, morphea. Morphea; When it affects the jaw area, it can cause skeletal and dental orthodontic malformations and tooth eruption delays. Morphea; The form with progressive hemifacial atrophy that can progress to the skin, subcutaneous tissues and bone is called Parry Romberg Syndrome. Parry Romberg syndrome is a neurocutaneous disorder. In this case report, rare extraoral and intraoral findings in a pediatric patient with Parry Romberg Syndrome are discussed.
References
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Referans1. Fett N, Werth VP. Update on morphea: part I. Epidemiology,
clinical presentation, and pathogenesis. J Am Acad Dermatol
2011;64:217–28.
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Referans2. Weibel L, Sampaio MC, Visentin MT, Howell KJ, Woo P,
Harper JI. Evaluation of methotrexate and corticosteroids for the
treatment of localized scleroderma (morphoea) in children. Br J
Dermatol 2006;155:1013–20.
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Referans3. Bhoyrul B, Clark S. Parry-Romberg syndrome and morphoea
en coup de sabre. Arch Dis Child 2019;104:400.
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Referans4. Misra R, Singh G, Aggarwal P, Aggarwal A. Juvenile onset
systemic sclerosis: a single center experience of 23 cases from
Asia. Clin Rheumatol 2007;26:1259–62.
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Referans5. Foeldvari I. Scleroderma in children. Curr Opin Rheumatol
2002;14:699–703.
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Referans6. Ullman S, Danielsen PL, Fledelius HC, Daugaard-Jensen
J, Serup J. Scleroderma en Coup de Sabre, Parry-romberg
hemifacial atrophy and associated manifestations of the eye, the
oral cavity and the teeth: a Danish follow-up study of 35 patients
diagnosed between 1975 and 2015. Dermatology 2021;237:204–
12.
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Referans7. Sevimli İ, Öztürk P, Mülayım MK, Nazik H, Geç Başlangıçlı
Lineer Skleroderma. Turkish J Fam Med Prim Care 12:153–5.
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Referans8. Holland KE, Steffes B, Nocton JJ, Schwabe MJ, Jacobson RD,
Drolet BA. Linear scleroderma en coup de sabre with associated
neurologic abnormalities. Pediatrics 2006;117:e132–6.
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Referans9. Wong M, Phillips CD, Hagiwara M, Shatzkes DR. Parry
Romberg syndrome: 7 cases and literature review. Am J
Neuroradiol 2015;36:1355–61.
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Referans10. 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.
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Referans11. Yim S, Yang I-H, Baek S-H. Characterization of dental
phenotypes and treatment modalities in Korean patients with
Parry-Romberg syndrome. Korean J Orthod 2020;50:407–17.
-
Referans12. Cui Y, Zhao J, Hu X, Fang B, Mao L. Combined Surgical-
Orthodontic Treatment of Patients With Severe Parry-Romberg
Syndrome. J Craniofac Surg 2022;33:e564–9.
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Referans13. Kumar NG, Maurya BS, Sudeep CS. Parry Romberg
syndrome: literature review and report of three cases. J Maxillofac
Oral Surg 2019;18:210–6.
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Referans14. Salimov F, Barış Ş, Dalili M, Koçak EF. Diş Mobilitesi ve
İmplant Stabilitesi için Kullanılan Ölçüm Yöntemleri. Arşiv Kaynak
Tarama Derg 2019;28:130–9.
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Referans15. Van der Cruyssen F, Meeus J, Schoenaers J, Politis C. Parry
Romberg syndrome: A long-term retrospective cohort study of 10
patients. Oral Maxillofac Surg Cases 2018;4:73–83.
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Referans16. Arif T, Majid I, Haji MLI. Late onset ‘en coup de sabre’following
trauma: Rare presentation of a rare disease. Our Dermatology
Online 2015;6:49.
-
Referans17. Brownell I, Soter NA. Familial linear scleroderma (en coup de
sabre) responsive to antimalarials and narrowband ultraviolet B
therapy. Dermatol Online J 2007;13.
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Referans18. Zulian F, Athreya BH, Laxer R, Nelson AM, Feitosa de Oliveira
SK, Punaro MG, et al. Juvenile localized scleroderma: clinical and
epidemiological features in 750 children. An international study.
Rheumatology 2006;45:614–20.
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Referans19. Müller L, van Waes H, Langerweger C, Molinari L, Saurenmann
RK. Maximal mouth opening capacity: percentiles for healthy
children 4–17 years of age. Pediatr Rheumatol 2013;11:1–7.
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Referans20. Hørberg M, Lauesen SR, Daugaard-Jensen J, Kjær I.
Linear scleroderma en coup de sabre including abnormal dental
development. Eur Arch Paediatr Dent 2015;16:227–31.
PARRY ROMBERG SENDROMLU PEDİATRİK BİR HASTANIN NADİR ORAL BULGULARI: BİR OLGU SUNUMU
Year 2024,
Volume: 13 Issue: 1, 155 - 160, 26.01.2024
Derya Sarıoğlu
,
Özge Anıl
Abstract
Skleroderma; kollajen yapım ve yıkımında ortaya çıkan bozukluklardan kaynaklanan, deri ve deri altı dokularda kalınlaşmaya ve sertleşmeye yol açan kronik bir hastalıktır. Pek çok alt tipi olan sklerodermanın çocuklarda en çok görülen tipi; lokalize sklerodermanın lineer formu, diğer bir deyişle morfeadır. Morfea; çene bölgesini etkilediği zaman, iskeletsel ve dişsel ortodontik malformasyonlara ve dişlerde sürme gecikmelerine neden olabilmektedir. Morfeanın; deri, deri altı dokulara ve kemiğe kadar ilerleyebilen progresif hemifasial atrofiyle seyreden formuna Parry Romberg Sendromu adı verilir. Parry Romberg sendromu nörokutanoz bir rahatsızlıktır. Bu vaka sunumunda, Parry Romberg Sendromu’na sahip pediatrik bir hastada görülen, nadir ekstraoral ve intraoral bulgulardan bahsedilmiştir.
References
-
Referans1. Fett N, Werth VP. Update on morphea: part I. Epidemiology,
clinical presentation, and pathogenesis. J Am Acad Dermatol
2011;64:217–28.
-
Referans2. Weibel L, Sampaio MC, Visentin MT, Howell KJ, Woo P,
Harper JI. Evaluation of methotrexate and corticosteroids for the
treatment of localized scleroderma (morphoea) in children. Br J
Dermatol 2006;155:1013–20.
-
Referans3. Bhoyrul B, Clark S. Parry-Romberg syndrome and morphoea
en coup de sabre. Arch Dis Child 2019;104:400.
-
Referans4. Misra R, Singh G, Aggarwal P, Aggarwal A. Juvenile onset
systemic sclerosis: a single center experience of 23 cases from
Asia. Clin Rheumatol 2007;26:1259–62.
-
Referans5. Foeldvari I. Scleroderma in children. Curr Opin Rheumatol
2002;14:699–703.
-
Referans6. Ullman S, Danielsen PL, Fledelius HC, Daugaard-Jensen
J, Serup J. Scleroderma en Coup de Sabre, Parry-romberg
hemifacial atrophy and associated manifestations of the eye, the
oral cavity and the teeth: a Danish follow-up study of 35 patients
diagnosed between 1975 and 2015. Dermatology 2021;237:204–
12.
-
Referans7. Sevimli İ, Öztürk P, Mülayım MK, Nazik H, Geç Başlangıçlı
Lineer Skleroderma. Turkish J Fam Med Prim Care 12:153–5.
-
Referans8. Holland KE, Steffes B, Nocton JJ, Schwabe MJ, Jacobson RD,
Drolet BA. Linear scleroderma en coup de sabre with associated
neurologic abnormalities. Pediatrics 2006;117:e132–6.
-
Referans9. Wong M, Phillips CD, Hagiwara M, Shatzkes DR. Parry
Romberg syndrome: 7 cases and literature review. Am J
Neuroradiol 2015;36:1355–61.
-
Referans10. 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.
-
Referans11. Yim S, Yang I-H, Baek S-H. Characterization of dental
phenotypes and treatment modalities in Korean patients with
Parry-Romberg syndrome. Korean J Orthod 2020;50:407–17.
-
Referans12. Cui Y, Zhao J, Hu X, Fang B, Mao L. Combined Surgical-
Orthodontic Treatment of Patients With Severe Parry-Romberg
Syndrome. J Craniofac Surg 2022;33:e564–9.
-
Referans13. Kumar NG, Maurya BS, Sudeep CS. Parry Romberg
syndrome: literature review and report of three cases. J Maxillofac
Oral Surg 2019;18:210–6.
-
Referans14. Salimov F, Barış Ş, Dalili M, Koçak EF. Diş Mobilitesi ve
İmplant Stabilitesi için Kullanılan Ölçüm Yöntemleri. Arşiv Kaynak
Tarama Derg 2019;28:130–9.
-
Referans15. Van der Cruyssen F, Meeus J, Schoenaers J, Politis C. Parry
Romberg syndrome: A long-term retrospective cohort study of 10
patients. Oral Maxillofac Surg Cases 2018;4:73–83.
-
Referans16. Arif T, Majid I, Haji MLI. Late onset ‘en coup de sabre’following
trauma: Rare presentation of a rare disease. Our Dermatology
Online 2015;6:49.
-
Referans17. Brownell I, Soter NA. Familial linear scleroderma (en coup de
sabre) responsive to antimalarials and narrowband ultraviolet B
therapy. Dermatol Online J 2007;13.
-
Referans18. Zulian F, Athreya BH, Laxer R, Nelson AM, Feitosa de Oliveira
SK, Punaro MG, et al. Juvenile localized scleroderma: clinical and
epidemiological features in 750 children. An international study.
Rheumatology 2006;45:614–20.
-
Referans19. Müller L, van Waes H, Langerweger C, Molinari L, Saurenmann
RK. Maximal mouth opening capacity: percentiles for healthy
children 4–17 years of age. Pediatr Rheumatol 2013;11:1–7.
-
Referans20. Hørberg M, Lauesen SR, Daugaard-Jensen J, Kjær I.
Linear scleroderma en coup de sabre including abnormal dental
development. Eur Arch Paediatr Dent 2015;16:227–31.