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Undifferentiated giant cell type carcinoma of the gallbladder with sarcomatoid dedifferentiation: a case report and review of the literature

机译:肉瘤样去分化的胆囊未分化巨细胞型癌:一例报道并文献复习

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Introduction Undifferentiated gallbladder carcinoma is a rare entity. Among unusual types of undifferentiated gallbladder carcinoma, giant cell type carcinoma is infrequent and, moreover, very few cases of such neoplasms with osteoclast-like giant cells have been documented. We report a case of undifferentiated gallbladder carcinoma presenting an unusual immunophenotype that was shown to be of giant cell type with sarcomatoid dedifferentiation infiltrated by osteoclast-like multinucleated cells. Case presentation An 84-year-old Greek man presented with right upper quadrant pain, high fever, rigors, anorexia and weight loss during the past month. Clinical examination revealed tenderness in the right upper abdominal quadrant and a palpable gallbladder. Blood tests showed elevated white blood-cell count and transaminases. Abdominal ultrasound and computed tomography demonstrated a markedly distended gallbladder, measuring 16 cm x 8 cm, with oedema and pericholecystic fluid, consistent with gallbladder empyema. After an open cholecystectomy and an uneventful recovery, the patient was discharged on the 4th postoperative day. On cut surface, a 2cm solid mass was identified, obstructing the lumen in the neck of the gallbladder. Histopathology and immunohistochemistry offered the diagnosis of an undifferentiated, giant cell type carcinoma of the gallbladder with sarcomatoid dedifferentiation infiltrated with osteoclast-like giant cells. Conclusions Undifferentiated, giant cell type carcinoma of the gallbladder with sarcomatoid dedifferentiation infiltrated with osteoclast-like giant cells is a very infrequent neoplasm. Controversy exists over its nature, as related knowledge remains incomplete. Thorough histopathological and immunohistochemical evaluation is imperative for diagnosis. Due to their rarity, the biological behaviour and prognosis of these tumours remain unclear.
机译:简介未分化的胆囊癌是一种罕见的实体。在异常类型的未分化胆囊癌中,巨细胞型癌很少见,而且,很少有这种破骨细胞样巨细胞瘤的病例报道。我们报告一例未分化的胆囊癌,表现出一种异常的免疫表型,该表型显示为破骨细胞样多核细胞浸润的肉瘤样去分化巨细胞型。病例介绍一名84岁的希腊男子在过去一个月内出现右上腹疼痛,高烧,严峻,厌食和体重减轻。临床检查显示右上腹象限有压痛,胆囊可触及。验血显示白细胞计数和转氨酶升高。腹部超声和计算机断层扫描显示胆囊明显扩张,大小为16 cm x 8 cm,并伴有水肿和胆囊液,与胆囊积脓相符。开腹胆囊切除术并恢复平稳后,患者于术后第4天出院。在切开的表面上,确认到2厘米的实心块,阻塞了胆囊颈部的内腔。组织病理学和免疫组织化学提供了诊断为未分化的胆囊巨细胞型癌,并伴有破骨细胞样巨细胞浸润的肉瘤样去分化。结论未分化的胆囊癌巨细胞型肉瘤样去分化并浸有破骨细胞样巨细胞癌是极少见的肿瘤。由于相关知识仍然不完整,因此就其性质存在争议。彻底的组织病理学和免疫组化评估对诊断至关重要。由于它们的稀有性,这些肿瘤的生物学行为和预后仍不清楚。

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