Nogales F F, Caballero T, Fernández P L, Linares J, Ruiz-Avila I
Department of Pathology, University of Granada Medical School, Spain.
Gynecol Oncol. 1991 Jan;40(1):78-80. doi: 10.1016/0090-8258(91)90090-r.
Pseudomyxoma peritonei associated with highly differentiated mucinous, intestinal-type ovarian tumor is reported in a 46-year-old acromegalic patient. Five years after its discovery a second operation revealed a mucinous cystadenoma of the appendix. The coexistence of pseudomyxoma peritonei with ovarian and appendicular tumors is rare, raising questions about the primary was origin of the peritoneal tumor. In this case the primary was ovarian while the appendicular tumor occurred later. Since acromegaly is associated with a high risk for the development of colorectal tumors, it could also have elicited a similar response in the intestinal-type ovarian tumor and the appendicular neoplasm found in this patient. The role of appendectomy in the surgical treatment and staging of ovarian tumors is stressed.
一名46岁的肢端肥大症患者被报道患有与高分化黏液性肠型卵巢肿瘤相关的腹膜假黏液瘤。发现该疾病五年后进行的第二次手术显示阑尾存在黏液性囊腺瘤。腹膜假黏液瘤与卵巢及阑尾肿瘤并存的情况较为罕见,这引发了关于腹膜肿瘤原发起源的疑问。在该病例中,原发部位是卵巢,而阑尾肿瘤是后来出现的。由于肢端肥大症与结直肠肿瘤发生的高风险相关,它也可能在该患者的肠型卵巢肿瘤和阑尾肿瘤中引发了类似反应。强调了阑尾切除术在卵巢肿瘤手术治疗及分期中的作用。