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副肿瘤天疱疮表现为侵袭性 T 细胞淋巴瘤的前驱症状。

Paraneoplastic pemphigus presenting as a prodrome to aggressive T cell lymphoma.

机构信息

Medicine, University of Florida, Gainesville, Florida, USA

University of Florida, Gainesville, Florida, USA.

出版信息

BMJ Case Rep. 2024 Jun 5;17(6):e258580. doi: 10.1136/bcr-2023-258580.

DOI:10.1136/bcr-2023-258580
PMID:38839409
Abstract

Paraneoplastic pemphigus (PNP) is a rare disease with an unclear mechanism of pathogenesis. We present a case of a male patient who presented with wound management after being diagnosed with Castleman disease-associated paraneoplastic pemphigus (PNP). The patient's condition was not improving; as a result, extensive workup was repeated, which confirmed the diagnosis of aggressive T cell lymphoblastic lymphoma. Our case signifies the importance of keeping a high index of suspicion for PNP-associated malignancies. This case report also adds emphasis to the diagnostic challenges faced by clinicians, making clinical correlation with multidisciplinary approach essential. Therefore, if clinically indicated, we need to revisit the diagnosis and seek alternative explanations to prevent delays in management.

摘要

副肿瘤天疱疮(PNP)是一种发病机制尚不清楚的罕见疾病。我们报告了一例男性患者,该患者在诊断为伴副肿瘤天疱疮(PNP)的Castleman 病后接受伤口处理。患者的病情没有改善;因此,反复进行了广泛的检查,最终确诊为侵袭性 T 细胞淋巴母细胞淋巴瘤。我们的病例表明,对 PNP 相关恶性肿瘤保持高度怀疑的重要性。本病例报告还强调了临床医生面临的诊断挑战,因此临床相关性和多学科方法至关重要。因此,如果临床上有指征,我们需要重新考虑诊断并寻找其他解释,以避免治疗延误。

相似文献

1
Paraneoplastic pemphigus presenting as a prodrome to aggressive T cell lymphoma.副肿瘤天疱疮表现为侵袭性 T 细胞淋巴瘤的前驱症状。
BMJ Case Rep. 2024 Jun 5;17(6):e258580. doi: 10.1136/bcr-2023-258580.
2
A case of paraneoplastic pemphigus associated with Castleman's disease.一例与卡斯特曼病相关的副肿瘤性天疱疮病例。
An Bras Dermatol. 2013 Nov-Dec;88(6 Suppl 1):11-4. doi: 10.1590/abd1806-4841.20132332.
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Paraneoplastic pemphigus associated with Castleman tumor, myasthenia gravis and bronchiolitis obliterans.副肿瘤性天疱疮伴发卡斯特曼病、重症肌无力和闭塞性细支气管炎。
J Am Acad Dermatol. 1999 Sep;41(3 Pt 1):393-400. doi: 10.1016/s0190-9622(99)70111-8.
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Paraneoplastic pemphigus associated with Castleman disease: A multicenter case series.副肿瘤性天疱疮合并 Castleman 病:多中心病例系列。
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Masked pemphigus among pediatric patients with Castleman's disease.Castleman病患儿中的隐匿性天疱疮。
Int J Rheum Dis. 2019 Jan;22(1):121-131. doi: 10.1111/1756-185X.13407. Epub 2018 Nov 8.
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Paraneoplastic pemphigus associated with Castleman's tumour.副肿瘤性天疱疮伴卡斯特曼病
Clin Exp Dermatol. 2000 May;25(3):219-21. doi: 10.1046/j.1365-2230.2000.00618.x.
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[Paraneoplastic pemphigus revealing dendritic cell sarcoma originating from Castleman's disease of the neck].[副肿瘤性天疱疮揭示起源于颈部Castleman病的树突状细胞肉瘤]
Ann Dermatol Venereol. 2005 Jan;132(1):41-4. doi: 10.1016/s0151-9638(05)79195-x.
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Paraneoplastic pemphigus caused by pre-existing stroma-rich variant of Castleman disease: from a pathologist's point of view.由先前存在的富于基质型 Castleman 病引起的副肿瘤性天疱疮:从病理学家的角度来看。
BMJ Case Rep. 2021 May 11;14(5):e241374. doi: 10.1136/bcr-2020-241374.
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Paraneoplastic Pemphigus. A Life-Threatening Autoimmune Blistering Disease.副肿瘤性天疱疮。一种危及生命的自身免疫性水疱病。
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Paraneoplastic pemphigus associated with follicular dendritic cell sarcoma arising from Castleman's tumor.与起源于Castleman病的滤泡树突状细胞肉瘤相关的副肿瘤性天疱疮。
J Am Acad Dermatol. 1999 Feb;40(2 Pt 2):294-7. doi: 10.1016/s0190-9622(99)70468-8.

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Paraneoplastic Pemphigus in a Patient With Pheochromocytoma: A Report of a Rare Case.嗜铬细胞瘤患者并发副肿瘤性天疱疮:1例罕见病例报告
Cureus. 2025 Feb 22;17(2):e79459. doi: 10.7759/cureus.79459. eCollection 2025 Feb.
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Autoimmune pemphigus: difficulties in diagnosis and the molecular mechanisms underlying the disease.自身免疫性天疱疮:诊断难点及疾病的分子机制
Front Immunol. 2025 Mar 3;16:1481093. doi: 10.3389/fimmu.2025.1481093. eCollection 2025.