Primary pure squamous cell carcinoma of the gall bladder – a case report of rare and aggressive entity with adverse prognosis

Mona Bargotya, A. Mehta, Payel Das, A. Sachan
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Abstract

Introduction. The most common malignancy of the biliary tract is gall bladder carcinoma and the main subtype according to the histological classification is Adenocarcinoma. Pure squamous cell carcinoma of the gall bladder is very rare entity accounting for only 1.1-3.7% of the gall bladder carcinomas. It is highly malignant with poor prognosis due to high proliferative rate and local invasiveness to the adjacent organs. The patients are usually diagnosed at an advanced stage with a bulky tumor owing to its aggressive behavior. Aim. In this paper, we describe a female patient with primary pure squamous cell carcinoma of the gall bladder. Description of the case. A 42-year old female patient presented with chief complaints of pain in abdomen associated with nausea and vomiting and gradually progressive jaundice since 02 months. Contrast Enhancing Computed Tomography (CECT) abdomen showed an enhancing mass lesion in gall bladder involving adjacent organs for which she underwent extended cholecystectomy with pancreaticoduodenectomy. Conclusion. Diagnosis as well as the management of this exceptionally rare type of tumour is undoubtedly challenging because of non-specific clinical as well as imaging findings. This case report is an attempt to add to the literary evidence for better pathological as well as clinical understanding of this rare and aggressive entity thereby providing additional material for the early diagnosis as well as the development of effective targeted therapies which will certainly help in increasing the lifespan of these patients.
原发性纯胆囊鳞状细胞癌-罕见侵袭性肿瘤1例,预后不良
介绍。胆道最常见的恶性肿瘤是胆囊癌,根据组织学分类,主要亚型为腺癌。单纯的胆囊鳞状细胞癌是一种非常罕见的肿瘤,仅占所有胆囊肿瘤的1.1-3.7%。由于高增殖率和局部侵犯邻近器官,它是高度恶性的,预后差。由于肿瘤具有侵袭性,患者通常在肿瘤晚期被诊断出来。的目标。在本文中,我们描述了一个女性患者原发性纯鳞状细胞癌的胆囊。案件描述。女,42岁,主诉腹部疼痛伴恶心呕吐,黄疸渐进性,02个月。腹部造影增强计算机断层扫描(CECT)显示胆囊肿块强化病变累及邻近器官,为此患者行胰十二指肠切除术及胆囊切除术。结论。由于非特异性的临床和影像学表现,这种异常罕见的肿瘤的诊断和治疗无疑具有挑战性。本病例报告试图增加文献证据,以更好地了解这种罕见的侵袭性实体的病理和临床,从而为早期诊断和有效靶向治疗的发展提供额外的材料,这将有助于延长这些患者的寿命。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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