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一名脾B细胞淋巴瘤患者并发副肿瘤性天疱疮和闭塞性细支气管炎

Paraneoplastic Pemphigus and Bronchiolitis Obliterans in a Patient with Splenic B-cell Lymphoma.

作者信息

Wang Shiou-Han, Chu Chia-Yu, Chen Hsuan-Hsiang, Chang Yih-Leong, Chen Kuan-Yu, Chiu Hsien-Ching

机构信息

Department of Dermatology, National Taiwan University Hospital, Taipei, Taiwan.

出版信息

J Formos Med Assoc. 2007 Sep;106(9):768-73. doi: 10.1016/S0929-6646(08)60038-8.

Abstract

Paraneoplastic pemphigus (PNP), also called paraneoplastic autoimmune multiorgan syndrome, is a rare disorder associated with underlying neoplasia. The common underlying neoplasms include non-Hodgkins lymphoma, chronic lymphocytic leukemia, and Castlemans disease. Though B-cell lymphoma is the most common underlying malignancy, only one case associated with splenic B-cell lymphoma has been recognized. The prognosis of PNP is very poor, and PNP-associated bronchiolitis obliterans (BO) is not uncommon. Herein, we report a 44-year-old woman who initially presented with multiple oral ulcers, conjunctivitis, and numerous cutaneous blisters. Serial workup established the diagnosis of PNP and revealed an underlying splenic B-cell lymphoma. Although the mucocutaneous lesions gradually healed after splenectomy and chemotherapy, deteriorating respiratory function developed 7 months later with pathologically proven BO. She finally succumbed to respiratory failure 12 months after presentation despite intensive respiratory care.

摘要

副肿瘤性天疱疮(PNP),也称为副肿瘤性自身免疫性多器官综合征,是一种与潜在肿瘤相关的罕见疾病。常见的潜在肿瘤包括非霍奇金淋巴瘤、慢性淋巴细胞白血病和卡斯特曼病。虽然B细胞淋巴瘤是最常见的潜在恶性肿瘤,但仅发现1例与脾B细胞淋巴瘤相关。PNP的预后很差,PNP相关的闭塞性细支气管炎(BO)并不少见。在此,我们报告一名44岁女性,最初表现为多处口腔溃疡、结膜炎和大量皮肤水疱。系列检查确立了PNP的诊断,并发现潜在的脾B细胞淋巴瘤。尽管脾切除和化疗后黏膜皮肤病变逐渐愈合,但7个月后呼吸功能恶化,病理证实为BO。尽管进行了强化呼吸护理,她最终在就诊12个月后死于呼吸衰竭。

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