Evacuation of axillary hematoma causing brachial plexus compression in newly diagnosed leukemia: a case report and literature review.

IF 0.6 Q4 SURGERY
Case Reports in Plastic Surgery and Hand Surgery Pub Date : 2026-02-23 eCollection Date: 2026-01-01 DOI:10.1080/23320885.2026.2636313
Isaac Mordukhovich, Hafsa Omer Sulaiman, Sean Frisbie, Anthony Tufaro, Bahar Bassiri Gharb, Antonio Rampazzo
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Abstract

Spontaneous soft tissue hematomas are recognized complications of myeloproliferative neoplasms but rarely implicate the brachial plexus. A large axillary hematoma could represent a surgical emergency due to compression of local neurovascular structures. We report a case of a 63-year-old male with a history of polycythemia vera who presented with an expansive axillary hematoma compressing his brachial plexus. The lesion's profound size caused upper limb paralysis and exquisite pain on passive movment, raised suspicion for malignant hematologic progression, and provided a localized etiology for the patient's plexopathy. Large-vessel compromise, central nervous system lesions, and soft tissue invasion were excluded by clinical evaluations and diagnostic imaging before the interdisciplinary decision was made to surgically evacuate the proven complex hematoma. The patient's pain improved following decompression and another washout two days later. Concurrent hematologic workup identified acute myelomonocytic leukemia by bone marrow biopsy and initiated appropriate management. Twenty-four abstracts were screened from PubMed using keyword search terms and citation matching. Thirteen patients were identified, 4 of which had compartment syndrome symptoms secondary to hematoma in the setting of an undiagnosed hematological malignancy. All cases in the literature were concurrently diagnosed with chronic myeloid leukemia whereas the case we present was a manifestation of acute myeloid leukemia. Extensive mass effect from a deep tissue hematoma as the chief complaint for a patient with leukemic transformation of polycythemia vera is a rare presentation. An interdisciplinary approach with meticulous hematologic workup allowed for management of both, the lesion's neuropathic mass effect and its underlying hematologic malignancy.

新诊断白血病腋窝血肿引流引起臂丛受压1例报告并文献复习。
自发性软组织血肿是公认的骨髓增生性肿瘤的并发症,但很少累及臂丛。一个大的腋窝血肿可能是由于压迫局部神经血管结构而引起的外科急诊。我们报告一例63岁男性真性红细胞增多症的历史谁提出了一个扩大腋窝血肿压迫他的臂丛。病变的巨大尺寸导致上肢瘫痪和被动运动时的剧烈疼痛,引起恶性血液学进展的怀疑,并为患者的神经丛病提供了局部病因。通过临床评估和诊断影像学排除大血管损害、中枢神经系统病变和软组织侵犯,然后做出跨学科的决定,手术清除已证实的复杂血肿。患者的疼痛在减压和两天后的另一次冲洗后得到改善。同时进行的血液学检查通过骨髓活检确定急性髓单核细胞白血病,并开始适当的治疗。使用关键词搜索和引文匹配从PubMed中筛选了24篇摘要。13例患者被确定,其中4例在未确诊的血液恶性肿瘤背景下继发于血肿的室间室综合征症状。所有的病例在文献中同时诊断为慢性髓性白血病,而我们目前的病例是急性髓性白血病的表现。深层组织血肿引起的广泛肿块效应是真性红细胞增多症白血病转化患者的主诉,这是一种罕见的表现。一个跨学科的方法与细致的血液学检查允许管理,病变的神经性肿块效应和其潜在的血液恶性肿瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
0.60
自引率
0.00%
发文量
40
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