Jatzko G R, Jester J
Surgical Department, Hospital of Barmherzige Brüder, St. Veit an der Glan, Austria.
Int J Colorectal Dis. 1997;12(6):326-8. doi: 10.1007/s003840050117.
Diffuse well differentiated papillary mesothelioma is a rare neoplasms of the peritoneal cavity which has generally been regarded as a tumor with low-grade malignant potential [1-4]. The well differentiated papillary mesotheliomas reported in recent literature are considered as border line lesions with a long term benign clinical course. There are however, only few studies with small numbers of diffuse well differentiated mesotheliomas [1, 2, 5, 6]. The synchronous appearance of such a lesion with a second malignancy therefore is a very rare event. Such a clinical scenario would suggest diffuse tumor spread to the peritoneum resulting in an inappropriate palliative procedure alone-being undertaken. To our knowledge this is the first report of the simultaneous occurrence of a rectal carcinoma in combination with a diffuse well differentiated papillary mesothelioma of the peritoneum.
弥漫性高分化乳头状间皮瘤是一种罕见的腹膜腔肿瘤,一般被认为是具有低恶性潜能的肿瘤[1-4]。近期文献报道的高分化乳头状间皮瘤被视为具有长期良性临床病程的交界性病变。然而,仅有少数关于少量弥漫性高分化间皮瘤的研究[1, 2, 5, 6]。因此,这种病变与第二种恶性肿瘤同时出现是非常罕见的事件。这样的临床情况提示肿瘤弥漫性播散至腹膜,从而仅采取了不恰当的姑息性手术。据我们所知,这是首例同时发生直肠癌合并腹膜弥漫性高分化乳头状间皮瘤的报告。