副肿瘤天疱疮合并b细胞淋巴瘤的多学科治疗1例。

IF 0.7 Q3 MEDICINE, GENERAL & INTERNAL
International Medical Case Reports Journal Pub Date : 2025-07-08 eCollection Date: 2025-01-01 DOI:10.2147/IMCRJ.S515068
Loulwah Alothman, Azizah Bin Mubayrik, Nuha Alfurayh, Sara Aldosary, Hend M Alotaibi, Abdulmajeed Alajlan
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引用次数: 0

摘要

背景:副肿瘤性天疱疮是一种罕见的危及生命的水疱性自身免疫性皮肤粘膜疾病,与多种肿瘤相关。与皮肤相比,粘膜病变是难治性的,需要相当长的愈合时间,愈合速度要慢得多。多学科的方法可以提供全面的管理和更好的预后。病例总结:一名61岁男性患者于2020年6月到急诊室就诊,主诉左眼严重炎症,并伴有手、躯干和脚的鳞状红斑性皮肤爆发。还观察到掌下血肿。临床检查发现广泛的口腔溃疡累及舌背、腹面、颊黏膜、唇黏膜,唇部可见血痂。患者因继发于穿孔性角膜溃疡的全眼炎入院。除了广泛的基线研究外,还要求进行皮肤病学调查以排除恶性肿瘤。患者腹膜后病变,接受CT引导活检。提示低级别B细胞非霍奇金淋巴瘤。他接受了血液肿瘤学、皮肤病学和口腔医学小组的治疗。结论:副肿瘤性天疱疮(PP)是一种与潜在恶性肿瘤相关的致死性自身免疫性水疱病。多学科的方法,以实现早期诊断和更好的管理是必不可少的,以提高生活质量的这类患者,尽管他们的预后不良。临床意义:副肿瘤性天疱疮是一种罕见的疾病,与皮肤粘膜溃疡和多种恶性肿瘤,包括淋巴增生性肿瘤有关。正如本例所示,多学科评估和管理已被证明在管理患者方面是有效的。医生和牙医应尽最大努力合作管理患者,尽量减少患者的痛苦,提高生活质量和预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multidisciplinary Management of Paraneoplastic Pemphigus Associated with B-Cell Lymphoma: A Case Report.

Background: Paraneoplastic pemphigus is a rare life-threatening blistering autoimmune mucocutaneous disease associated with various neoplasms. In contrast to the skin, mucosal lesions are refractory and requires considerable healing time, heals far more slowly. A multidisciplinary approach may provide a comprehensive management and a better prognosis.

Case summary: A sixty-one-year-old male patient presented to the ER department in June 2020 complaining of severe inflammation of the left eye along with scaly erythematous skin eruptions affecting the hands, trunk, and feet. Subungual hematoma was also observed. Clinical examination revealed extensive oral ulceration involving the dorsum and ventral surface of the tongue, buccal mucosa, labial mucosa, and hematic crusts were noticed on the lips. The patient was admitted for panophthalmitis secondary to a perforated corneal ulcer. Dermatological investigations were requested in addition to extensive baseline studies to rule out malignancies. The patient had a retroperitoneal lesion and underwent CT guided biopsy. Result was suggestive of low-grade B cell non-Hodgkin's lymphoma. He was treated by the haematology-oncology, dermatology and oral medicine teams.

Conclusion: Paraneoplastic pemphigus (PP) is a fatal autoimmune blistering disease associated with underlying malignancy. A multidisciplinary approach to achieve early diagnosis and better management is essential to improve the quality of life of such patients despite their poor prognosis.

Clinical significance: Paraneoplastic pemphigus is a rare disease associated with mucocutaneous ulcerations and various malignancies, including lymphoproliferative neoplasms. As demonstrated in the current case, multidisciplinary assessment and management have proven to be effective in managing the patient. Physicians and dentists should make their best effort to work collaboratively to manage patients and minimize patient distress and improve life quality and prognosis.

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来源期刊
International Medical Case Reports Journal
International Medical Case Reports Journal MEDICINE, GENERAL & INTERNAL-
CiteScore
1.40
自引率
0.00%
发文量
135
审稿时长
16 weeks
期刊介绍: International Medical Case Reports Journal is an international, peer-reviewed, open access, online journal publishing original case reports from all medical specialties. Submissions should not normally exceed 3,000 words or 4 published pages including figures, diagrams and references. As of 1st April 2019, the International Medical Case Reports Journal will no longer consider meta-analyses for publication.
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