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  • 1 Borsod-Abaúj-Zemplén Megyei Központi Kórház és Egyetemi Oktatókórház, Miskolc, Szentpéteri kapu 72–76., 3526
  • 2 Debreceni Egyetem, Debrecen
Open access

Absztrakt:

A Parry–Romberg-szindróma ritka, lassan progrediáló, autolimitált betegség, melyet unilateralis arcfélatrophia jellemez. Általában gyerek-, fiatal felnőtt korban manifesztálódik. Az atrophia mértékének, illetve a társuló egyéb tünetek változatosságának következtében a betegség diagnózisa, a prognózis megítélése és a kezelés nagy kihívást jelent. Az esetbemutatás célja rávilágítani a diagnózis felállításának nehézségeire, bemutatni a beteg kivizsgálásának lépéseit, felhívni a figyelmet a műtét megfelelő időzítésének fontosságára, a hemifacialis atrophia mértékének megfelelő műtét kiválasztására, illetve a szindrómával gyakran előforduló betegségek keresésére. Orv Hetil. 2020; 161(28): 1181–1185.

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  • 1

    Sharma M, Bharatha A, Antonyshyn OM, et al. Case 178: Parry–Romberg syndrome. Radiology 2012; 262: 721–725.

  • 2

    Rangare AL, Babu SG, Thomas PS, et al. Parry–Romberg syndrome: a rare case report. J Oral Maxillofac Res. 2011; 2: e5.

  • 3

    Gupta S, Mathur M. “The unkindest cut of all”: Parry–Romberg syndrome – an unwonted affair. J Clin Diagn Res. 2016; 10: TJ01–TJ02.

  • 4

    Wong M, Phillips CD, Hagiwara M, et al. Parry–Romberg syndrome: 7 cases and literature review. Am J Neuroradiol. 2015; 36: 1355–1361.

  • 5

    Chen JT, Eisinger B, Esguibel C, et al. Changes in cutaneous gene expression after microvascular free tissue transfer in Parry–Romberg syndrome. Plast Reconstr Surg. 2018; 142: 303e–309e.

  • 6

    di Meo N, Stinco G, Nan K, et al. Parry–Romberg syndrome: a case with a possible association with Lyme disease. Acta Dermatovenorol Alp Pannonica Adriat. 2015; 24: 77–79.

  • 7

    Sahin MT, Bariş S, Karaman A. Parry–Romberg syndrome: a possible association with borreliosis. J Eur Acad Dermatol Venereol. 2004; 18: 204–207.

  • 8

    Gutiérrez-Gómez C, Godínez-Hana AL, García-Hernández M, et al. Lack of IgG antibody seropositivity to Borrelia burgdorferi in patients with Parry–Romberg syndrome and linear morphea en coup de sabre in Mexico. Int J Dermatol. 2014; 53: 947–951.

  • 9

    Latha S, Shefali J, Jaideep S, et al. Parry–Romberg syndrome: a case report and review. Int J Appl Dent Sci. 2016; 2: 75–78.

  • 10

    Haldar A, Mukherjee A. Parry–Romberg’s disease with intractable partial epilepsy. Neurol India 2007; 55: 160–162.

  • 11

    Gulati S, Jain V, Garg G. Parry–Romberg syndrome. Indian J Pediatr. 2006; 73: 448–449.

  • 12

    Madasamy R, Jayanandan M, Adhavan UR, et al. Parry–Romberg syndrome: a case report and discussion. J Oral Maxillofac Pathol. 2012; 16: 406–410.

  • 13

    Bucher F, Fricke J, Neugebauer A, et al. Ophthalmological manifestations of Parry–Romberg syndrome. Surv Ophthalmol. 2016; 61: 693–701.

  • 14

    Chhabra A, Lam JM, Rhemus W. Tongue involvement in Parry–Romberg syndrome. J Rheumatol. 2017; 44: 1412.

  • 15

    Khan M, Khan M, Negi R, et al. Parry–Romberg syndrome with localized scleroderma: a case report. J Clin Exp Dent. 2014; 6: e313–e316.

  • 16

    Kiss VP, Pere T, Karagity E, et al. Localised scleroderma on face (en coup de sabre) – case report. [Lokalizált scleroderma arcon (en coup de sabre) – betegbemutatás.] Bőrgyógy Venerol Szle. 2017; 93: 39–41. [Hungarian]

  • 17

    Stone J. Parry–Romberg syndrome. Pract Neurol. 2006; 6: 185–188.

  • 18

    Patel H, Thakkar C, Patel K. Parry–Romberg syndrome: a rare entity. J Maxillofac Oral Surg. 2010; 9: 247–250.

  • 19

    Tollefson MM, Witman PM. En coup de sabre morphea and Parry–Romberg syndrome: a retrospective review of 54 patients. J Am Acad Dermatol. 2007; 56: 257–263.

  • 20

    Sommer A, Gambichler T, Bacharach-Buhles M, et al. Clinical and serological characteristics of progressive facial hemiatrophy: a case series of 12 patients. J Am Acad Dermatol. 2006; 54: 227–233.

  • 21

    Korkmaz C, Adapinar B, Uysal S. Beneficial effect of immunosuppressive drugs on Parry–Romberg syndrome: a case report and review of the literature. South Med J. 2005; 98: 940–942.

  • 22

    Guerrerosantos J, Guerrerosantos F, Orozco J. Classification and treatment of facial tissue atrophy in Parry–Romberg disease. Aesthetic Plast Surg. 2007; 31: 424–434.

  • 23

    Agostini T, Spinelli G, Marino G, et al. Esthetic restoration in progressive hemifacial atrophy (Romberg disease): structural fat grafting versus local/free flaps. J Craniofac Surg. 2014; 25: 783–787.

  • 24

    Chen JT, Schmid DB, Siebert JW. A 26-year experience with microsurgical reconstruction of hemifacial atrophy and linear scleroderma. Plast Reconstr Surg. 2018; 142: 1275–1283.

  • 25

    Simonacci F, Bertozzi N, Grieco MP, et al. Procedure, applications, and outcomes of autologous fat grafting. Ann Med Surg. 2017; 20: 49–60.

  • 26

    Balaji SM. Subdermal fat grafting for Parry–Romberg syndrome. Ann Maxillofac Surg. 2014; 4: 55–59.

  • 27

    Sterodimas A, Huanquipaco JC, Filho SS, Autologous fat transplantation for the treatment of Parry–Romberg syndrome. J Plast Reconstr Aesthet Surg. 2009; 62: e424–e426.

  • 28

    Asai S, Kamei Y, Nishibori K, et al. Reconstruction of Romberg disease defects by omental flap. Ann Plast Surg. 2006; 57: 154–158.

  • 29

    Hunstad JP, Shifrin DA, Kortesis BG. Successful treatment of Parry–Romberg syndrome with autologous fat grafting: 14-year follow-up and review. Ann Plast Surg. 2011; 67: 423–425.

  • 30

    Koh KS, Oh TS, Kim H, et al. Clinical application of human adipose tissue-derived mesenchymal stem cells in progressive hemifacial atrophy (Parry–Romberg disease) with microfat grafting techniques using 3-dimensional computed tomography and 3-dimensional camera. Ann Plast Surg. 2012; 69: 331–337

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