Titlebook: Management of Blistering Diseases; Fenella Wojnarowska,Robert A. Briggaman Book 1990 Springer Science+Business Media Dordrecht 1990 diseas

Aids209

https://doi.org/10.1007/978-1-4899-7190-6disease; diseases; management

Aboveboard

tendinitis

CHOP

Bullous pemphigoidacterized histologically by subepidermal bullae and immunopathologically by . deposition of autoantibodies and complement components along the epidermal basement membrane zone (BMZ). The majority of these patients also have circulating autoantibodies directed against the BMZ of stratified squamous e

圖表證明

Cicatricial pemphigoidnding on the tissues involved, this disease has been referred to by a variety of names including ocular pemphigoid, chronic cicatricial conjunctivitis, essential shrinkage of the conjunctivae, oral pemphigoid and benign mucous membrane pemphigoid. In addition, it is occasionally incorrectly referred

使成波狀

Herpes gestationisle and choriocarcinoma. There is a considerable clinical and pathological overlap between HG and the pemphigoid group of disorders. In view of this the disorder is now frequently termed pemphigoid gestationis [1,2].

white-matter

Epidermolysis bullosa acquisitault onset and an absence of a family history of epidermolysis bullosa [1–3]. The term, acquired epidermolysis bullosa (EBA), was coined to categorize this group [1,3]. In order to tighten the diagnosis, Roenigk . [4], in 1971 proposed the following clinical criteria for the disease: (1) trauma-induc

legitimate

輕浮思想

Diagnosis and diagnostic techniquess are life-threatening conditions and others are associated with chronic disability and pain. Parents of affected children may be committed to dedicated nursing care and subject to all the frustrations of having a disabled child. They may also have to live with anxiety over the risk of having furthe

itinerary

Epidermolysis bullosa simplex (intraepidermal epidermolysis bullosa) and allied conditions [1]. K?bner in 1886 called the same condition epidermolysis bullosa hereditaria (EBH) [2]. Since the latter term soon became adopted for several congenital traumatic blistering diseases, Hallopeau [3] found it necessary to call the original type’ simple’, i. e. epidermolysis bullosa simplex (EBS).