Atas Hakan, Bulus Hakan, Akkurt Göhan
Department of General Surgery, Ankara Numune Training and Research Hospital, Ankara, Turkey.
Department of General Surgery Kecioren Training and Research Hospital, Ankara, Turkey.
Euroasian J Hepatogastroenterol. 2017 Jan-Jun;7(1):89-91. doi: 10.5005/jp-journals-10018-1221. Epub 2017 May 5.
Sclerosing angiomatoid nodular transformation (SANT) is a rare and benign lesion arising from the red pulp of the spleen, with an unknown etiopathogenesis. These tumors are usually asymptomatic or cause nonspecific abdominal pain. Most SANTs are found incidentally on radiographic examination, or during surgery for an unrelated condition. Therefore, high clinical suspicion is of great importance for the diagnosis. Splenectomy provides complete cure, and no recurrence and/or malignant transformation was reported to date. In this study, a rare case of SANT was reported in a young adult male, and was discussed with the relevant literature. Atas H, Bulus H, Akkurt G. Sclerosing Angiomatoid Nodular Transformation of the Spleen: An uncommon Cause of Abdominal Pain. Euroasian J Hepato-Gastroenterol 2017;7(1):89-91.
硬化性血管瘤样结节性转化（SANT）是一种罕见的良性病变，起源于脾脏红髓，病因不明。这些肿瘤通常无症状或引起非特异性腹痛。大多数SANT是在影像学检查中偶然发现的，或在因无关疾病进行手术时发现的。因此，高度的临床怀疑对诊断至关重要。脾切除术可实现完全治愈，迄今为止尚未有复发和/或恶变的报道。在本研究中，报告了一例年轻成年男性的罕见SANT病例，并结合相关文献进行了讨论。阿塔斯H、布卢斯H、阿克库尔特G。脾脏硬化性血管瘤样结节性转化：腹痛的罕见原因。《欧亚肝脏胃肠病学杂志》2017年；7(1):89 - 91。
