Pathology department, Nanjing JunXie Hospital, Nanjing, China.
Translational Medicine Center, Nanjing JunXie Hospital, Nanjing, China.
Medicine (Baltimore). 2022 Dec 30;101(52):e32528. doi: 10.1097/MD.0000000000032528.
Inflammatory pseudotumor-like follicular dendritic cell sarcoma (IPT-like FDCS) is often associated with Epstein-Barr (EB) virus infection. The tumor is commonly found in the spleen and liver, and it has been reported in the literature that it can be associated with paraneoplastic pemphigus, myasthenia gravis, and other diseases. A case of IPT-like FDCS with clinical features of thrombocytopenia has not been reported.
A 59-year-old male patient visited our hospital in September 2020 due to bleeding gums and epistaxis.
Splenic lymphoma with marked thrombocytopenia was initially diagnosed. The patient underwent pathological examination after splenectomy. Microscopic examination showed spindle-shaped or oval cells arranged in loose bundles, a large number of lymphocytes and plasma cells infiltrating the interstitium, and fibrin-like changes in the blood vessel wall. Immunohistochemical detection of tumor cells was positive for CD21, CD35, and Epstein-Barr virus in situ hybridization, and the patient was diagnosed with IPT-like FDCS.
The patient underwent a splenectomy. The patient received platelet-raising therapy postoperatively.
No tumor recurrence or metastasis was found during the 17-month follow-up period, and the platelet count returned to normal.
IPT-like FDCS is an uncommon tumor, and its first presentation with marked thrombocytopenia is even rarer. The tumor was clinically and radiographically nonspecific. Definitive diagnosis relies on histopathological and immunohistochemical staining. IPT-like FDCS is biologically indolent and has a favorable prognosis.
炎症性假瘤样滤泡树突状细胞肉瘤(IPT 样 FDCS)常与 Epstein-Barr(EB)病毒感染有关。肿瘤常见于脾脏和肝脏,文献中已有报道称其可与副肿瘤性天疱疮、重症肌无力等疾病相关。具有血小板减少症临床表现的 IPT 样 FDCS 尚未见报道。
一位 59 岁男性患者于 2020 年 9 月因牙龈出血和鼻出血就诊于我院。
初步诊断为伴有明显血小板减少的脾淋巴瘤。患者行脾切除术后行病理检查。镜下见梭形或椭圆形细胞呈疏松束状排列,间质内大量淋巴细胞和浆细胞浸润,血管壁呈纤维蛋白样改变。肿瘤细胞免疫组化检测 CD21、CD35 阳性,原位杂交检测 EBV 阳性,诊断为 IPT 样 FDCS。
患者行脾切除术。术后给予升血小板治疗。
患者随访 17 个月,未发现肿瘤复发或转移,血小板计数恢复正常。
IPT 样 FDCS 是一种罕见肿瘤,其首发表现为明显血小板减少症更为罕见。该肿瘤在临床上和影像学上均无特异性。明确诊断依赖于组织病理学和免疫组织化学染色。IPT 样 FDCS 生物学行为惰性,预后良好。