自发性肿瘤溶解综合征是胸腺瘤伴外周血淋巴细胞增多症的罕见表现

IF 0.4 Q3 MEDICINE, GENERAL & INTERNAL Proceedings of Singapore Healthcare Pub Date : 2022-04-01 DOI:10.1177/20101058221089989
L. Nyanti, Andy Sing Ong Tang, Adam Ismail, L. Chew, T. S. Leong
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引用次数: 0

摘要

肿瘤溶解综合征在血液系统恶性肿瘤中很常见,但在实体瘤中很少报道。外周血淋巴细胞增多症是胸腺瘤的一种自身免疫性特征。我们报告了一位63岁的女性,她表现为纵隔肿块、自发性肿瘤溶解综合征和外周血片上的白细胞成红细胞图像。骨髓抽吸和环钻活检排除了血液恶性肿瘤。纵隔肿块的活检证实了胸腺瘤。这是第一例报道的胸腺瘤合并外周血淋巴细胞增多并伴有自发性肿瘤溶解综合征的病例。临床医生被提醒,在外周血淋巴细胞增多症的情况下,实体瘤可能会伪装成血液系统恶性肿瘤,因此需要仔细的临床评估来区分这两种诊断。
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Spontaneous tumour lysis syndrome as a rare presentation of thymoma with peripheral blood lymphocytosis
Tumour lysis syndrome is common in haematological malignancies but is rarely reported in solid tumours. Peripheral blood lymphocytosis is an autoimmune feature of thymomas. We report a 63-year-old female who presented with a mediastinal mass, spontaneous tumour lysis syndrome and a leukoerythroblastic picture on peripheral blood film. Bone marrow aspiration and trephine biopsy ruled out haematological malignancy. Subsequent biopsy of the mediastinal mass confirmed thymoma. This is the first reported case of thymoma with peripheral blood lymphocytosis presenting with spontaneous tumour lysis syndrome. Clinicians are reminded that solid tumours may masquerade as haematological malignancies in the presence of peripheral blood lymphocytosis, hence careful clinical evaluation is needed to differentiate between the two diagnoses.
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来源期刊
Proceedings of Singapore Healthcare
Proceedings of Singapore Healthcare MEDICINE, GENERAL & INTERNAL-
CiteScore
0.90
自引率
0.00%
发文量
42
审稿时长
15 weeks
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