Tilakaratne Wm, Dissanayake M
Department of Oral Pathology, Faculty of Dental Sciences, University of Peradeniya, Sri Lanka.
Oral Dis. 2005 Sep;11(5):326-9. doi: 10.1111/j.1601-0825.2005.01116.x.
Paraneoplastic pemphigus (PNP) is an autoimmune mucocutaneous disease frequently associated with lymphoproliferative disorders. The rare combination of the disease with other malignancies such as different types of carcinomas, sarcomas, melanoma and skin tumours has also been reported. Most patients develop very severe oral ulceration and conjunctival ulceration with or without genital ulceration resembling the features of Steven's Johnson's syndrome or most severe forms of drug eruptions. The possibility of PNP should be borne in mind when a patient presents with extensive oral ulceration if clinical, histopathological and results of direct immunofluorescence are not pathognomonic for a specific diagnosis. The issue becomes even more important as some patients with PNP have no diagnosed malignancy at the time of presentation. We document a case of PNP in a 29-year-old female who suffers from non-Hodgkin's lymphoma.
副肿瘤性天疱疮(PNP)是一种常与淋巴增殖性疾病相关的自身免疫性黏膜皮肤疾病。该疾病与其他恶性肿瘤(如不同类型的癌、肉瘤、黑色素瘤和皮肤肿瘤)的罕见组合也有报道。大多数患者会出现非常严重的口腔溃疡和结膜溃疡,有或无生殖器溃疡,类似于史蒂文斯-约翰逊综合征或最严重形式的药物疹的特征。如果临床、组织病理学和直接免疫荧光结果不能明确诊断某种特定疾病,那么当患者出现广泛口腔溃疡时,应考虑PNP的可能性。由于一些PNP患者在就诊时未被诊断出患有恶性肿瘤,这个问题就变得更加重要。我们记录了一例患有非霍奇金淋巴瘤的29岁女性的PNP病例。