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先天性无纤维蛋白原血症患者出现腿部溃疡。

Leg ulcer presenting in a patient with congenital afibrinogenaemia.

作者信息

Kinebuchi Akira, Ohtsuka Tsutomu, Ishida Shinnosuke, Otsuka Shun, Abe Takako, Yamakage Akio, Yamazaki Soji, Nakamura Yuichiro, Hirota Ken

机构信息

Department of Dermatology, Dokkyo University School of Medicine, 880 Kitakobayashi, Mibu, Tochigi 321-0293, Japan.

出版信息

Eur J Dermatol. 2002 Jan-Feb;12(1):70-2.

Abstract

Congenital afibrinogenaemia is a rare hemorrhagic disorder characterized by the absence of fibrinogen. We report a case of congenital afibrinogenaemia presented with leg ulcer. A 30-year-old man presented with a history of prolonged bleeding from birth. His parents are cousins. He repeatedly showed haematoma after traumas on his leg. He was diagnosed as having congenital afibrinogenaemia because of plasma fibrinogen deficiency. Because his leg ulcer gradually increased in size, he was admitted to our department for treatment. Laboratory examinations revealed prolonged bleeding time, prolonged coagulation time, prolonged prothrombin time, prolonged activated partial thromboplastin time and plasma fibrinogen was not measurable. Histological examination revealed hyperkeratosis, acanthosis and severe fibrotic change in the whole dermis. Severe hemosiderin deposit was found in the middle dermis. His leg ulcer cured 2 months after the beginning of fresh frozen plasma administration (FFP), but recurrence of the leg ulcer after FFP treatment was found. This is the second reported case of congenital afibrinogenaemia presented with leg ulcer.

摘要

先天性无纤维蛋白原血症是一种罕见的出血性疾病,其特征是缺乏纤维蛋白原。我们报告一例以腿部溃疡为表现的先天性无纤维蛋白原血症病例。一名30岁男性有自出生起出血时间延长的病史。他的父母是近亲。他腿部外伤后反复出现血肿。因血浆纤维蛋白原缺乏,他被诊断为先天性无纤维蛋白原血症。由于其腿部溃疡面积逐渐增大,他入住我科接受治疗。实验室检查显示出血时间延长、凝血时间延长、凝血酶原时间延长、活化部分凝血活酶时间延长,且血浆纤维蛋白原无法测出。组织学检查显示全层真皮有角化过度、棘层肥厚和严重纤维化改变。真皮中层发现严重含铁血黄素沉积。新鲜冰冻血浆输注开始2个月后其腿部溃疡治愈,但发现新鲜冰冻血浆治疗后腿部溃疡复发。这是第二例报告的以腿部溃疡为表现的先天性无纤维蛋白原血症病例。

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