Asiyanbola Bolanle, Camuto Patricia, Mansourian Vazrik
Department of Pathology, Hospital of Saint Raphael, New Haven, CT 06511, USA.
J Gastrointest Surg. 2006 May;10(5):657-61. doi: 10.1016/j.gassur.2005.09.015.
Malakoplakia, characterized by histiocytes with Michaelis-Gutmann bodies, is a rare entity. It is particularly so in the gastrointestinal tract, where it has been described in association with colon cancer, with about 20 cases described worldwide. The significance of this condition lies in its potential effect upon the preoperative staging and treatment of associated colorectal cancer. Its presence may lead to preoperative clinical and radiological over staging and more extensive resection, as well as the use of neoadjuvant therapy or a decision to undertake palliative care. This condition is more common in males. We present the case of the oldest reported patient with this association. The patient was a 90-year-old female who was treated with a sigmoid resection for an obstructing sigmoid lesion. At operation, the left ureter was embedded within an inflammatory pericolic mass but was not grossly involved with tumor. The tumor was a Dukes' stage B adenocarcinoma and occurred in association with malakoplakia.
以含有迈克尔is - 古特曼小体的组织细胞为特征的软斑病是一种罕见的病症。在胃肠道中尤为罕见,在胃肠道中它已被描述为与结肠癌相关,全球范围内约有20例相关报道。这种情况的意义在于它可能对相关结直肠癌的术前分期和治疗产生影响。它的存在可能导致术前临床和影像学过度分期以及更广泛的切除,以及使用新辅助治疗或决定进行姑息治疗。这种情况在男性中更常见。我们报告了有这种关联的年龄最大的患者病例。该患者是一名90岁女性,因乙状结肠梗阻性病变接受了乙状结肠切除术。手术时,左输尿管包埋在炎性结肠周围肿块内,但未被肿瘤明显累及。肿瘤为杜克B期腺癌,与软斑病相关。