原发性血小板增多症作为多神经病变、器官肿大、内分泌病变、m蛋白、皮肤改变综合征的初始表现,对硼替佐米、环磷酰胺、地塞米松方案完全有效:1例报告。

IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL
Alireza Zangooie, Zahra Moradi, Reza Asgari, Amirhosein Maharati, Zahra Salehi, Abolghasem Allahyari
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引用次数: 0

摘要

背景:多发性神经病变、器官肿大、内分泌病变、m蛋白、皮肤改变综合征是一种罕见的副肿瘤疾病,常表现为不典型症状,使诊断具有挑战性。本病例为罕见的原发性血小板增多症,最初表现为多发性神经病变、器官肿大、内分泌病变、m蛋白、皮肤改变综合征。此外,它强调了显著的治疗反应,在硼替佐米、环磷酰胺、地塞米松方案治疗后实现了完全缓解,强调了这种联合治疗在治疗此类复杂病例中的疗效。病例介绍:一名65岁伊朗妇女,表现为疲劳、头痛和血小板增多,诊断为原发性血小板增多症。随着时间的推移,她的病情随着神经病变的发展和血小板增多的持续而恶化,这需要进一步的调查。影像学显示多发性淋巴结病变、硬化性骨病变及腹水,怀疑为浆细胞病变。骨髓活检、淋巴结活检和血管内皮生长因子水平升高证实诊断为多神经病变、器官肿大、内分泌病变、m蛋白、皮肤改变综合征。患者给予硼替佐米、环磷酰胺、地塞米松化疗方案治疗,症状完全缓解,全血细胞计数正常化,影像学表现明显改善。结论:本病例强调需要识别非典型多神经病变、器官肿大、内分泌病变、m蛋白、皮肤变化综合征表现,如原发性血小板增多症,及时诊断,并强调硼替佐米、环磷酰胺、地塞米松方案在完全缓解中的疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Essential thrombocythemia as an initial presentation of polyneuropathy, organomegaly, endocrinopathy, M-protein, skin changes syndrome with complete response to the bortezomib, cyclophosphamide, dexamethasone regimen: a case report.

Background: Polyneuropathy, organomegaly, endocrinopathy, M-protein, skin changes syndrome is a rare paraneoplastic disorder often presenting with atypical manifestations, making diagnosis challenging. This case is novel due to the rare presentation of essential thrombocythemia as the initial manifestation of polyneuropathy, organomegaly, endocrinopathy, M-protein, skin changes syndrome. Furthermore, it highlights the remarkable therapeutic response, achieving a complete remission following treatment with the bortezomib, cyclophosphamide, dexamethasone regimen, underscoring this combination therapy's efficacy in managing such complex cases.

Case presentation: A 65-year-old Iranian woman presented with fatigue, headache, and thrombocytosis, leading to a diagnosis of essential thrombocythemia. Over time, her condition progressed with the development of neuropathy and persistence of thrombocytosis, which warranted further investigation. Imaging revealed multiple lymphadenopathies, sclerotic bone lesions, and ascitic fluid, raising suspicion for a plasma cell dyscrasia. Bone marrow biopsy, lymph node biopsy, and elevated vascular endothelial growth factor levels confirmed the diagnosis of polyneuropathy, organomegaly, endocrinopathy, M-protein, skin changes syndrome. The patient was treated with bortezomib, cyclophosphamide, dexamethasone chemotherapy regimen, resulting in complete symptom relief, normalization of the complete blood count, and significant improvement in imaging findings.

Conclusion: This case highlights the need to recognize atypical polyneuropathy, organomegaly, endocrinopathy, M-protein, skin changes syndrome presentations, such as essential thrombocythemia, for timely diagnosis and underscores the bortezomib, cyclophosphamide, dexamethasone regimen's efficacy in achieving complete remission.

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来源期刊
Journal of Medical Case Reports
Journal of Medical Case Reports Medicine-Medicine (all)
CiteScore
1.50
自引率
0.00%
发文量
436
期刊介绍: JMCR is an open access, peer-reviewed online journal that will consider any original case report that expands the field of general medical knowledge. Reports should show one of the following: 1. Unreported or unusual side effects or adverse interactions involving medications 2. Unexpected or unusual presentations of a disease 3. New associations or variations in disease processes 4. Presentations, diagnoses and/or management of new and emerging diseases 5. An unexpected association between diseases or symptoms 6. An unexpected event in the course of observing or treating a patient 7. Findings that shed new light on the possible pathogenesis of a disease or an adverse effect
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