毛细胞白血病表现为胸前软组织肿块1例并文献复习

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Khaled A. Murshed, A. Fadul, M. Yassin, F. Hilmi, A. Elsayed, I. Al-Bozom
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引用次数: 0

摘要

图1所示。18F-FDG静脉注射304mbq后1小时的PET/CT扫描显示,以前纵隔为中心的不规则浸润性纵隔软组织肿块,延伸至胸骨前皮下区域,沿胸膜背侧向膈脚延伸,双侧肋膈前纵隔淋巴结伴fdg阳性。摘要:毛细胞白血病(HCL)是一种罕见的慢性淋巴细胞增生性疾病。最初的表现通常包括与外周血细胞减少有关的症状。它有时有非典型的表现,可以出现在不寻常的部位。我们报告一个不寻常的HCL表现为胸骨前软组织肿块在一个45岁的男人。他的外周血计数显示全血细胞减少。未见明显淋巴结或肝脾肿大。ct扫描显示中纵隔肿块并延伸至胸骨前软组织。组织核心活检和组织病理学结果证实了HCL的诊断。据我们所知,这是第二例报道的HCL表现为胸骨前软组织肿块。虽然罕见,但在涉及髓外/结外部位(包括软组织和骨骼)肿瘤的鉴别诊断中应考虑HCL,因此患者可以在治疗反应性疾病的早期诊断中获得最大的益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hairy Cell Leukemia Presenting as Presternal Soft Tissue Mass: A Case Report With Review of Literature
FIGURE 1. PET/CT scan 1 hour after the IV administration of 304 MBq of 18F-FDG showed an irregular, infiltrative mediastinal soft tissue mass centered on the anterior mediastinum with extensions to the presternal subcutaneous region and towards the diaphragmatic crura along the dorsal aspects of the pleura with FDG-avid bilateral anterior costophrenic mediastinal lymph nodes. Abstract: Hairy cell leukemia (HCL) is an uncommon chronic lymphoproliferative disorder. Initial presentation frequently includes symptoms related to peripheral blood cytopenias. It can sometimes have atypical manifestations and can present at unusual sites. We report an unusual presentation of HCL as a presternal soft tissue mass in a 45-year-old man. His peripheral blood counts showed pancytopenia. There were no palpable lymph nodes or hepatosplenomegaly. CT-scan revealed a middle mediastinal mass with extension into the presternal soft tissue. Tissue core biopsy was taken and histopathologic findings confirmed the diagnosis of HCL. To our knowledge, this is the second reported case of HCL presenting as a presternal soft tissue mass. Although rare, HCL should be considered in the differential diagnosis of tumors involving extramedullary/extranodal sites including the soft tissue and bone, so the patient can get the utmost benefit for early diagnosis of a treatment responsive disease.
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期刊介绍: Each issue of Pathology Case Reviews examines one vital theme in the field with peer-reviewed, clinically oriented case reports that focus on diagnosis, specimen handling and reports generation. Each theme-oriented issue covers both histopathologic and cytopathologic cases, offering a comprehensive perspective that includes editorials and review articles of the newest developments in the field, differential diagnosis hints, applications of new technologies, reviews of current issues and techniques and an emphasis on new approaches.
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