Clement P B, Young R H, Scully R E
Department of Pathology, Vancouver Hospital and Health Sciences Centre, Canada.
Am J Surg Pathol. 1996 Sep;20(9):1067-80. doi: 10.1097/00000478-199609000-00004.
Nine cases of malignant mesothelioma (MM) presenting as ovarian masses occurred in female patients aged 16 to 63 (median, 52) years. In most of the cases, the referring pathologist initially misdiagnosed the neoplasm or was uncertain about its nature. In two cases, the tumors were confined to one or both ovaries, representing primary ovarian MMs; only one similar case has been previously reported. In the other cases, widespread peritoneal tumor precluded definite conclusions about the primary or secondary nature of the ovarian involvement. That at least some of the latter were also primary ovarian MMs is suggested by a degree of ovarian enlargement, the striking parenchymal replacement, or both, which are not usually seen in cases of secondary ovarian involvement by peritoneal MMs. The clinical presentation was usually that of abdominal or pelvic pain or abdominal swelling, an adnexal mass on pelvic examination or at laparotomy, or combinations thereof. One tumor was an autopsy finding. There was no history of asbestos exposure in any patient. Eight patients underwent bilateral oophorectomy, usually with hysterectomy and biopsies of extraovarian tumor. Four patients were given chemotherapy and one, radiation therapy. Follow-up in five cases revealed that three patients had died of tumor at postoperative intervals of 8 to 44 months, one was alive with persistent tumor at 18 months, and one was alive with no clinical evidence of tumor at 11 years. The ovaries were replaced by tumors 3 to 15 cm in maximum diameter; seven were bilateral. The neoplastic tissue was typically solid, but small cysts were present in two cases, and one tumor was a unilocular cyst with a solid mural nodule. On microscopic examination, tumor involved both the serosa and the parenchyma of the ovary in seven cases, the serosa only in one case, and the parenchyma only in one case. Seven tumors were exclusively epithelial, with papillary, tubular-glandular, and solid patterns, and two were biphasic. The cells in the epithelial mesotheliomas usually exhibited moderate atypicality and a low mitotic rate. The stroma was typically hyalinized, and in three of the cases with a papillary pattern papillae with hyalinized cores were a striking finding. Psammoma bodies were present in three cases. Histochemical and immunohistochemical stains confirmed the mesothelial nature of the tumor cells. Because of the wide variety of microscopic patterns in MMs, the differential diagnosis of ovarian MM includes a variety of primary and metastatic ovarian tumors as well as other peritoneal mesothelial lesions.
9例表现为卵巢肿块的恶性间皮瘤(MM)发生于16至63岁(中位年龄52岁)的女性患者。在大多数病例中,转诊的病理学家最初误诊了该肿瘤或对其性质不确定。2例中,肿瘤局限于一侧或双侧卵巢,代表原发性卵巢MM;此前仅报道过1例类似病例。在其他病例中,广泛的腹膜肿瘤使关于卵巢受累的原发性或继发性性质难以得出明确结论。卵巢至少有一定程度的增大、显著的实质替代,或两者兼而有之,提示至少部分后者也是原发性卵巢MM,而腹膜MM累及卵巢的继发性病例通常不会出现这些表现。临床表现通常为腹痛或盆腔痛、腹部肿胀、盆腔检查或剖腹手术时发现附件肿块,或上述情况的组合。1例肿瘤为尸检发现。所有患者均无石棉接触史。8例患者接受了双侧卵巢切除术,通常同时行子宫切除术及卵巢外肿瘤活检。4例患者接受了化疗,1例接受了放疗。5例患者的随访结果显示,3例患者在术后8至44个月死于肿瘤,1例在18个月时仍有持续性肿瘤存活,1例在11年时存活且无肿瘤的临床证据。卵巢被最大直径3至15 cm的肿瘤取代;7例为双侧性。肿瘤组织通常为实性,但2例有小囊肿,1例为单房囊肿,囊壁有实性结节。显微镜检查显示,7例患者肿瘤累及卵巢的浆膜和实质,1例仅累及浆膜,1例仅累及实质。7例肿瘤仅为上皮性,呈乳头状、管状腺状和实性结构,2例为双相性。上皮性间皮瘤细胞通常表现为中度异型性和低有丝分裂率。间质通常透明变性,在3例乳头状结构的病例中,有透明变性核心的乳头是一个显著特征。3例有砂粒体。组织化学和免疫组织化学染色证实了肿瘤细胞的间皮性质。由于MM的显微镜下模式多种多样,卵巢MM的鉴别诊断包括多种原发性和转移性卵巢肿瘤以及其他腹膜间皮病变。