Sitaraman Lalitha M, Linn John G, Matkowskyj Kristina A, Wayne Jeffrey D
Feinberg School of Medicine;
Rare Tumors. 2010 Sep 30;2(3):e46. doi: 10.4081/rt.2010.e46.
We report a case of sclerosing angiomatoid nodular transformation (SANT) of the spleen presenting as an incidental splenic mass in a patient with a history of retroperitoneal spindle cell sarcoma. Imaging studies and preoperative fine needle biopsy failed to differentiate this lesion from other vascular splenic lesions or a metastatic focus of a prior sarcoma. The patient was treated with splenectomy, which has proved both diagnostic and therapeutic in this and other cases of SANT. Although histology can lead to the diagnosis of vascular tumor, immunohistochemistry is the only way to confirm the diagnosis of SANT. The etiology of SANT is unknown. SANT of the spleen is a benign lesion that does not recur after splenectomy.
我们报告一例脾脏硬化性血管瘤样结节性转化(SANT)病例,该病例表现为一名有腹膜后梭形细胞肉瘤病史患者的脾脏偶然肿块。影像学检查和术前细针活检未能将此病变与其他脾脏血管性病变或既往肉瘤的转移灶区分开来。该患者接受了脾切除术,在本病例及其他SANT病例中,脾切除术已证明具有诊断和治疗作用。虽然组织学检查可诊断血管肿瘤,但免疫组织化学是确诊SANT的唯一方法。SANT的病因尚不清楚。脾脏SANT是一种良性病变,脾切除术后不会复发。