scholarly journals Oromandibular Limb Hypogenesis Syndrome Type I B as a Rare Clinical Variant: A Case Report and Review of the Literature

2019 ◽  
Vol 7 (1) ◽  
Author(s):  
Azam Hosseini ◽  
Shabnam Sohanian
Keyword(s):  
Case Report ◽  
Type I ◽  
Syndrome Type ◽  
Review Of The Literature ◽  
Clinical Variant

Bilateral duane’s syndrome Type I in siblings: Case Report

2020 ◽  
pp. 271-275
Author(s):  
C. Schiavi ◽  
M. Fresina ◽  
F. Quagliano ◽  
E.C. Campos
Keyword(s):  
Case Report ◽  
Type I ◽  
Syndrome Type ◽  
Duane’S Syndrome

Familial Eruptive Syringomas: Case Report and Review of the Literature

2013 ◽  
Vol 17 (2) ◽  
pp. 84-88 ◽  
Author(s):  
Jenny Lau ◽  
Richard M. Haber
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Rare Clinical Entity ◽  
Benign Neoplasms ◽  
Review Of The Literature ◽  
Causative Gene ◽  
Unusual Condition ◽  
Clinical Variant ◽  
Insight Into

Background: Syringomas are benign neoplasms of eccrine origin. A clinical variant is eruptive syringomas, which presents as firm, smooth, yellow to pigmented papules that appear as successive crops on the neck, axillae, chest, abdomen, and/or periumbilical region. To our knowledge, there are only 10 published reports of familial eruptive syringomas. Herein we describe the eleventh report of familial eruptive syringomas, review the literature on this unusual presentation, and suggest a novel classification of familial syringomas based on our literature review. Observations: We report two cases of eruptive syringoma within a family. Eruptive syringomas were widely distributed on the trunk of a healthy 16-year-old female and her 19-year-old brother. Both the 19-year-old man and his mother also had infraorbital syringomas. Conclusion: Familial eruptive syringomas are a rare clinical entity that is likely autosomal dominantly inherited. Future reports of this unusual condition may provide further insight into the etiology of familial syringomas, and genetic analysis of cases may enable the causative gene mutation to be determined.

Primary gastric T-cell lymphoma not associated with human T-lymphotropic virus type I: a case report and review of the literature

2003 ◽  
Vol 82 (3) ◽  
pp. 197-202 ◽  
Author(s):  
N. Niitsu ◽  
H. Nakamine ◽  
M. Kohri ◽  
M. Hayama ◽  
J. Tamaru ◽  
...  
Keyword(s):  
Case Report ◽  
T Cell ◽  
Virus Type ◽  
Cell Lymphoma ◽  
T Cell Lymphoma ◽  
Type I ◽  
Review Of The Literature ◽  
T Lymphotropic Virus

Isotretinoin for the Treatment of Granulomatous Rosacea: Case Report and Review of the Literature

2012 ◽  
Vol 16 (6) ◽  
pp. 438-441 ◽  
Author(s):  
Efstathios Rallis ◽  
Chrysovalantis Korfitis
Keyword(s):  
Case Report ◽  
Clinical Course ◽  
Nous Rapportons ◽  
Review Of The Literature ◽  
Granulomatous Rosacea ◽  
Clinical Variant ◽  
Oral Isotretinoin ◽  
Granulomatous Disorders

Background: Granulomatous rosacea is considered a clinical variant of rosacea and is characterized by hard yellow, brown, red or flesh-colored cutaneous papules or nodules that may be severe and may lead to scarring. The lesions typically appear on the cheeks and periorificial lesions; they are monomorphic in each patient and sit on relatively normal-appearing skin. The diagnosis should be established by excluding other granulomatous disorders and rosacea-like eruptions such as sarcoidosis, tuberculosis, and lupus miliaris disseminatus faciei. The clinical course is chronic and unpredictable, and management can be very difficult. Case Report: We report the case of a 28-year-old female with granulomatous rosacea who responded successfully to oral isotretinoin. No recurrence was noticed 6 months after the completion of treatment. Renseignements de base: La rosacée granulomateuse est considérée comme une variante clinique de la rosacée et est caractérisée par la présence de papules cutanées jaunes, brunes, ou fleshed-colored rouges dures ou par de nodules qui peuvent être graves et qui peuvent causer des cicatrices. Les lésions sont généralement localisées aux joues et sur les lésions péri-orificielles; elles sont monomorphes chez chaque patient individuel et elles siègent sur une peau d'apparence relativement normale. Le diagnostic doit être établi en excluant les autres troubles granulomateux et les éruptions rosacéiformes comme la sarcoïdose, la tuberculose, et la tuberculide papulonodulaire. L'évolution clinique est chronique et imprévisible, et la gestion peut être très difficile. Rapport de cas: Nous rapportons le cas d'une femme âgée de 28 ans présentant une rosacée granulomateuse qui a été traité avec succès avec l'isotrétinoïne administrée par voie orale. Aucune récidive n'a été observée 6 mois après la fin du traitement.

Oral-facial-digital syndrome type I: Surgical approach and a case report

2014 ◽  
Vol 67 (3) ◽  
pp. 396-398 ◽  
Author(s):  
M. García González ◽  
M. Pombo Castro ◽  
D. Vela Nieto ◽  
J. Caramés Bouzán
Keyword(s):  
Case Report ◽  
Surgical Approach ◽  
Type I ◽  
Syndrome Type

Psoriasis vulgaris and autoimmune polyendocrine syndrome type I: a case report

2014 ◽  
Vol 27 (7-8) ◽  
Author(s):  
Atilla Cayir ◽  
Ragıp Ismail Engin ◽  
Mehmet Ibrahim Turan ◽  
Erdal Pala
Keyword(s):  
Case Report ◽  
Psoriasis Vulgaris ◽  
Type I ◽  
Syndrome Type ◽  
Autoimmune Polyendocrine Syndrome
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