Pretibial Epidermolysis Bullosa

نویسنده

  • Dr. C. K. Ho
چکیده

History A 12-year-old boy presented with a history of blistering due to trauma on both shins since birth. They healed with scarring and milia formation. The lesions mainly affected the shins and some occasionally appeared on the waist. They were mildly pruritic and were worse in the summer as well as being precipitated by trauma. There was also toenail dystrophy but his hair and teeth were normal. He had been treated with a combination of topical steroid (clobetasol propionate) and antifungal cream (clotrimazole) leading to some improvement. There was no mucosal involvement. There was no significant medical history and he was not on any regular medication. His mother had similar nail changes but no skin lesions. His maternal uncle also had similar lesions on the shins but none of his immediate family was affected. Date: 10 January, 2001 Venue: Yaumatei Dermatology Clinic Organizer: Social Hygiene Service, DH; Clinico-pathological Seminar Physical examination On examination, there were isolated blisters on both shins with adjacent scarring, milia and lichenoid papules (Figure 1). There was nail dystrophy on both feet (Figure 2). His mucosa and dentition were normal. General examination was normal. The differential diagnosis included pretibial epidermolysis bullosa, bullous lichen planus, bullous lupus erythematosus and bullous pemphigoid.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Pretibial Epidermolysis Bullosa: Report of two cases

Pretibial epidermolysis bullosa is a rare variant of hereditary epidermolysis bullosa characterized by the delayed onset of lesions and their localization. We present two cases, a 35-year-old woman and a 21-year-old man. They clinically had pruritus, nodular prurigo-like or lichenified lesions, violaceous scarring, milia, nail dystrophy and in one case albopapuloid lesions on the trunk. Physica...

متن کامل

Elephantiasic Pretibial Myxedema in Graves' Disease:Report of Two Cases

Pretibial myxedema (PTM) is usually a late manifestation of Graves' disease and is relatively rare. The elephantiasis nostras variant comprises less than one percent of patient with pretibial myxedema. We report two cases of elephantiasic PTM and review the literature regarding its treatment. Therapy of the elephantiasic variant of PTM remains suboptimal at present. ( J Intern Med Taiwan 2004; ...

متن کامل

Microsoft Word - NEF331BF.rtf

Occurrence of Hereditary Nephritis, Pretibial Epidermolysis bullosa and Beta-Thalassemia minor in Two Siblings with End-Stage Renal Disease A. Alexander Kagan S. Steven Feld J. Juan Chemke Y. Yaacov Bar-Khayim Division of Nephrology, Department of Internal Medicine B, and Clinical Genetics Unit, Kaplan Hospital (affiliated to the Medical School of the Hebrew University and Hadassah, Jerusalem),...

متن کامل

180 - kD Bullous Pemphigoid Antigen ( BP 180 ) Is Deficient in Generalized Atrophic Benign Epidermolysis Bullosa Marcel

Introduction Generalized atrophic benign epidermolysis bullosa (GABEB) is a form of nonlethal junctional epidermolysis bullosa characterized by universal alopecia and atrophy of the skin. We report a deficiency of the 180-kD bullous pemphigoid antigen in three patients with GABEB from unrelated families. We screened specimens of clinically normal skin from nine junctional epidermolysis bullosa ...

متن کامل

Clinical variability in dystrophic epidermolysis bullosa and findings with scanning electron microscopy.

In dystrophic epidermolysis bullosa, the genetic defect of anchoring fibrils leads to cleavage beneath the basement membrane and its consequent loss. A 46 year-old female patient presented blisters with a pretibial distribution associated with nail dystrophy. Her two children had hyponychia and anonychia, which affected all toe nails and the thumb, forefinger and middle finger. DNA sequencing i...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2001