Ramteke Prashant, Iyer Venkat K, Madan Karan, Gamangatti Shivanand, Mridha Asit R
Department of Pathology, All India Institute of Medical Sciences, New Delhi, India.
Department of Pulmonary Medicine and Sleep Disorders, All India Institute of Medical Sciences, New Delhi, India.
J Cytol. 2017 Jul-Sep;34(3):174-176. doi: 10.4103/0970-9371.208111.
Tenosynovial giant cell tumors (TGCTs) arise from the synovium of joint, bursa, and tendon sheath, and are classified into localized and diffuse types. Diffused type often affects the large joint, and has more recurrence, metastasis, and malignant transformation potential compared to the localized type. Malignant diffused TGCT (D-TGCT) usually occurs as a large tumor (>5 cm), in older patients, and its histopathologic features include necrosis, cellular anaplasia, prominent nucleoli, high nuclear cytoplasmic ratio, brisk mitosis, discohesion of tumor cells, paucity of giant cells, and a diffuse growth pattern. At least five of these criteria are required for the histopathologic diagnosis of malignant TGCT because the benign TGCT also shares many of these morphological features. We describe the cytomorphologic features of a malignant D-TGCT from an unusual case of pulmonary metastasis in an adult patient. Fine needle aspiration cytologic features of malignant D-TGCT have not been described earlier in the English literature.
腱鞘巨细胞瘤(TGCTs)起源于关节、滑囊和腱鞘的滑膜,分为局限性和弥漫性两种类型。弥漫性类型常累及大关节,与局限性类型相比,具有更高的复发、转移和恶变潜能。恶性弥漫性TGCT(D-TGCT)通常表现为较大的肿瘤(>5cm),多见于老年患者,其组织病理学特征包括坏死、细胞间变、核仁突出、核质比高、有丝分裂活跃、肿瘤细胞离散、巨细胞稀少以及弥漫性生长模式。由于良性TGCT也具有许多这些形态学特征,因此恶性TGCT的组织病理学诊断至少需要满足其中五项标准。我们描述了一例成年患者发生肺转移的罕见恶性D-TGCT的细胞形态学特征。英文文献中此前尚未描述过恶性D-TGCT的细针穿刺细胞学特征。