Gupta Rakesh K, Saran Ravindra K, Srivastava Arvind K, Jagetia Anita, Garg Lalit, Sharma Mehar C
Department of Pathology, G B Pant Institute of Postgraduate Medical Education and Research, New Delhi, India.
Department of Neurosurgery, G B Pant Institute of Postgraduate Medical Education and Research, New Delhi, India.
Neuropathology. 2017 Aug;37(4):358-364. doi: 10.1111/neup.12375. Epub 2017 Mar 13.
We present a rare case of primary pituitary T cell lymphoma/leukemia (T-LBL) in association with adrenocorticotropic hormone (ACTH) and thyroid stimulating hormone (TSH) expressing pituitary adenoma in a 55-year-old woman highlighting the importance of intra-operative squash smears examination. The patient presented with complaints of headache, diminution of vision and recent onset altered sensorium. MRI revealed a mass lesion in the sellar-suprasellar region with non-visualization of pituitary gland separately, extending to involve adjacent structures diagnosed as invasive pituitary macroadenoma. Intra-operative tissue was sent for squash smear examination. The cytology showed a tumor comprising of sheets of immature lymphoid cells intermixed with clusters of pituitary acinar cells with many mitoses and tingible body macrophages. A diagnosis of presence of immature lymphoid cells within the pituitary was offered and differentials of infiltration by lymphoma cells from systemic disease versus primary central nervous lymphoma-like lymphoma arising in the pituitary adenoma were considered. Later paraffin section examination and immunohistochemistry corroborated with the squash findings and a final diagnosis of primary pituitary T cell lymphoma/leukemia in association with ACTH and TSH expressing pituitary adenoma was made. To date, only six cases of primary pituitary T cell lymphomas, including three T-LBL cases, have been reported. This is the seventh case and first one additionally describing cytohistological correlation and importance of intra-operative cytology.
我们报告了一例罕见的原发性垂体T细胞淋巴瘤/白血病(T-LBL),该病例发生在一名55岁女性身上,与表达促肾上腺皮质激素(ACTH)和促甲状腺激素(TSH)的垂体腺瘤相关,强调了术中压片涂片检查的重要性。患者出现头痛、视力减退以及近期意识改变的症状。磁共振成像(MRI)显示蝶鞍-鞍上区域有一个肿块病变,垂体无法单独显示,病变延伸累及相邻结构,诊断为侵袭性垂体大腺瘤。术中送检组织进行压片涂片检查。细胞学检查显示肿瘤由成片的未成熟淋巴细胞与垂体腺泡细胞簇混合组成,有许多有丝分裂象和吞噬含铁血黄素巨噬细胞。初步诊断为垂体存在未成熟淋巴细胞,并考虑了来自全身性疾病的淋巴瘤细胞浸润与垂体腺瘤中发生的原发性中枢神经系统淋巴瘤样淋巴瘤的鉴别诊断。随后的石蜡切片检查和免疫组化结果与压片涂片结果相符,最终诊断为原发性垂体T细胞淋巴瘤/白血病合并表达ACTH和TSH的垂体腺瘤。迄今为止,仅报道了6例原发性垂体T细胞淋巴瘤,其中包括3例T-LBL病例。这是第7例,也是第一例额外描述细胞组织学相关性及术中细胞学重要性的病例。