Alizadeh Mehdi, Vafaie Majid, Tarlan Saeid, Moeini Hossein, Chelkassri Fatemeh Mohammadi, Khoeiniha Mohammad Hosein, Fathi Seyed Mohammad, Didban Abdollah, Chegini Victoria
Children Growth Research Center, Research Institute for Prevention of Non-Communicable Diseases, Qazvin University of Medical Sciences, Ghods Hospital, Shahid Beheshti Blvd, Qazvin, 3415914595, Iran.
Respir Med Case Rep. 2020 Dec 8;31:101312. doi: 10.1016/j.rmcr.2020.101312. eCollection 2020.
Thymolipoma is a benign and rare tumor that could be found at any age. Thymolipoma associated with the myasthenia gravis, Graves disease, aplastic anemia, and hypogammaglobulinemia was reported previously, but in this case, thymolipoma is associated with lymphocytosis. A 6-year-old girl was brought to the hospital because of a chronic cough. Her evaluation revealed a 130 × 160× 160 mm fat-containing soft tissue mass arising from anterior mediastinum with complete left lung collapse and contralateral mediastinal shift. Her past medical history showed that she had been evaluated and treated unsuccessfully due to severe lymphocytosis two years earlier. Her peripheral blood and bone marrow cell morphology were normal; in contrast, blood cell count and CD flow cytometry showed severe lymphocytosis. The patient's tumor was excised entirely without any complications, and lymphocytosis resolved during the follow-up period. Because the T lymphocytes are developed in the thymus, and more than 80% of cells in CD flow cytometry were T lymphocytes, and the lymphocytosis resolved with tumor removal; therefore, the authors suggested that Thymolipoma could be associated with lymphocytosis.
胸腺脂肪瘤是一种良性罕见肿瘤,可在任何年龄发现。此前有胸腺脂肪瘤与重症肌无力、格雷夫斯病、再生障碍性贫血及低丙种球蛋白血症相关的报道,但在本病例中,胸腺脂肪瘤与淋巴细胞增多症相关。一名6岁女孩因慢性咳嗽被送至医院。检查发现前纵隔有一个130×160×160mm含脂肪的软组织肿块,导致左肺完全萎陷及对侧纵隔移位。她的既往病史显示,两年前她因严重淋巴细胞增多症接受评估和治疗但未成功。她的外周血和骨髓细胞形态正常;相反,血细胞计数和CD流式细胞术显示严重淋巴细胞增多症。患者的肿瘤被完整切除,无任何并发症,且淋巴细胞增多症在随访期间得以缓解。由于T淋巴细胞在胸腺中发育,且CD流式细胞术中80%以上的细胞为T淋巴细胞,且淋巴细胞增多症随肿瘤切除而缓解;因此,作者认为胸腺脂肪瘤可能与淋巴细胞增多症有关。