Gilks C B, Young R H, Aguirre P, DeLellis R A, Scully R E
Department of Pathology, University of British Columbia, Vancouver, Canada.
Am J Surg Pathol. 1989 Sep;13(9):717-29. doi: 10.1097/00000478-198909000-00001.
We reviewed 26 examples of the rare variant of cervical adenocarcinoma that has been designated "adenoma malignum." The patients, three of whom had Peutz-Jeghers syndrome, ranged in age from 25 to 72 years (average, 42 years). The most common presenting symptom was menometrorrhagia, followed by vaginal discharge, postmenopausal bleeding, and abdominal swelling in decreasing order of frequency. In 12 of the patients, the diagnosis was established on the basis of the examination of a cervical biopsy specimen, endocervical curettage specimen, or both. In three of these cases, however, up to four biopsies were performed before the diagnosis was established. In the remaining 14 patients, the diagnosis was not made until the time of operation or pathologic examination of a hysterectomy specimen. On gross examination, the cervix usually appeared abnormal, but occasional specimens were considered unremarkable. The cervix was typically described as firm or indurated. Microscopic examination showed glands that were irregular in size and shape and lined predominantly by mucin-containing columnar epithelial cells with basal nuclei. The tumors typically exhibited deep invasion of the cervical wall, and a portion of the infiltrating tumor was associated with a stromal response in most cases. Minor foci of tumor with a less well-differentiated appearance were present in 15 of the 26 tumors. Argyrophil cells were present in six of 15 tumors. Five of the six tumors containing argyrophil cells stained immunohistochemically for serotonin and peptide hormones. Positive staining for serotonin was seen in four tumors; one of these also contained a few cells positive for neurotensin. Cytoplasmic staining of the tumor cells for carcinoembryonic antigen (CEA) was seen in five of six cases. CEA reactivity was very focal in two of the positive tumors. Microscopic features that were most helpful in distinguishing adenoma malignum from normal endocervix or benign endocervical glandular proliferations were the presence of markedly irregular, abnormally shaped glands; invasion of the cervical wall; a loose edematous or desmoplastic stromal response; foci of less well-differentiated tumor; vascular invasion; perineural invasion; and positive staining for CEA. Despite radical therapy in most of the cases, the prognosis was poor. Follow-up data were available for 22 patients. Thirteen of them died of recurrent tumor, four were alive with recurrent tumor at the time of last follow-up examination, and only three patients were disease free for 2 years or more.4+ tumor of the
我们回顾了26例被命名为“恶性腺瘤”的宫颈腺癌罕见变异型病例。患者年龄在25至72岁之间(平均42岁),其中3例患有佩-吉综合征。最常见的症状是月经过多,其次是阴道分泌物、绝经后出血和腹部肿胀,其出现频率依次降低。12例患者通过宫颈活检标本、宫颈管刮除术标本或两者检查确诊。然而,其中3例在确诊前进行了多达4次活检。其余14例患者直到手术时或子宫切除标本的病理检查时才确诊。大体检查时,宫颈通常外观异常,但偶尔有标本看似正常。宫颈通常被描述为质地坚硬或硬结。显微镜检查显示腺体大小和形状不规则,主要由含黏液的柱状上皮细胞衬里,细胞核位于基底。肿瘤通常表现为宫颈壁深层浸润,大多数情况下,部分浸润性肿瘤伴有间质反应。26例肿瘤中有15例存在分化较差的小灶性肿瘤。15例肿瘤中有6例存在嗜银细胞。含嗜银细胞的6例肿瘤中有5例免疫组化检测血清素和肽类激素呈阳性。4例肿瘤血清素染色呈阳性;其中1例还含有少数神经降压素阳性细胞。6例中有5例肿瘤细胞癌胚抗原(CEA)呈细胞质染色阳性。2例阳性肿瘤中CEA反应非常局限。有助于将恶性腺瘤与正常宫颈管或良性宫颈管腺体增生区分开来的显微镜特征包括:存在明显不规则、形状异常的腺体;宫颈壁浸润;疏松水肿或促纤维组织增生的间质反应;分化较差的肿瘤灶;血管浸润;神经周围浸润;以及CEA染色阳性。尽管大多数病例采用了根治性治疗,但预后较差。有22例患者的随访数据。其中13例死于肿瘤复发,4例在最后一次随访检查时仍有复发性肿瘤存活,只有3例患者无病生存2年或更长时间。4 +肿瘤