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液体及细针穿刺标本中颗粒细胞瘤的细胞学特征。

Cytologic features of granulosa cell tumors in fluids and fine needle aspiration specimens.

作者信息

Lal Aseem, Bourtsos Eleni P, Nayar Ritu, DeFrias Denise V

机构信息

Department of Pathology, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.

出版信息

Acta Cytol. 2004 May-Jun;48(3):315-20. doi: 10.1159/000326379.

Abstract

OBJECTIVE

To describe the cytologic features of granulosa cell tumors in fluids and fine needle aspiration specimens, with histologic confirmation.

STUDY DESIGN

Histologically confirmed granulosa cell tumors, 6 adult type and 1 juvenile type, were identified. All patients had local recurrences or metastases. Eleven specimens from 7 patients, including cytologic samples, cell blocks and histology, were reviewed. Inhibin immunostaining was performed on cell blocks to aid identification of this group of tumors in the cytologic and histologic samples.

RESULTS

The patients were 22-72 years old. Sites included ovary and peritoneum; there were pelvic recurrences and metastatic lesions in the spleen, liver, perirectum and cervical lymph node. Cytologic features of adult granulosa cell tumors included 3-dimensional clusters, resettes loose monolayers and individual cells. Other features were Call-Exner bodies, vacuolated cytoplasm, exuberant capillaries associated with papillarylike fronds, a second population of elongated theca cells, and prominent or rare nuclear grooves. In juvenile granulosa cell tumor the features observed were monolayers, loosely cohesive sheets, single cells, occasional larger pleomorphic cells with nuclear clefting and nuclear protrusions, vacuolated cytoplasm, finely granular chromatin and frequent mitoses. The overall cytologic and histologic correlation was good. Inhibin was focally positive in one peritoneal fluid, correlating with the focal pattern of staining seen on histology.

CONCLUSION

A definitive cytologic diagnosis of granulosa cell tumor can be made based on the above criteria. Aggressive tumors are discohesive and show pleomorphism and nuclear protrusions. Inhibin stain may be helpful in identifying granulosa cell tumors in cell block specimens.

摘要

目的

描述在液体和细针穿刺标本中颗粒细胞瘤的细胞学特征,并进行组织学确认。

研究设计

确定了6例成人型和1例青少年型经组织学确诊的颗粒细胞瘤。所有患者均有局部复发或转移。对7例患者的11份标本进行了回顾,包括细胞学样本、细胞块和组织学检查。对细胞块进行抑制素免疫染色,以辅助在细胞学和组织学样本中识别这组肿瘤。

结果

患者年龄在22至72岁之间。病变部位包括卵巢和腹膜;有盆腔复发以及脾脏、肝脏、直肠周围和颈部淋巴结的转移病灶。成人颗粒细胞瘤的细胞学特征包括三维细胞团、菊形团、松散的单层细胞和单个细胞。其他特征有Call-Exner小体、空泡状细胞质、与乳头状叶相关的丰富毛细血管、第二种细长的卵泡膜细胞群体以及明显或罕见的核沟。青少年颗粒细胞瘤观察到的特征为单层细胞、松散黏附的片层、单个细胞、偶尔有较大的多形性细胞伴有核裂和核突出、空泡状细胞质、细颗粒状染色质和频繁的有丝分裂。总体细胞学与组织学相关性良好。在一份腹腔积液中抑制素呈局灶性阳性,与组织学上看到的局灶性染色模式相关。

结论

根据上述标准可对颗粒细胞瘤做出明确的细胞学诊断。侵袭性肿瘤细胞黏附性差,表现出多形性和核突出。抑制素染色可能有助于在细胞块标本中识别颗粒细胞瘤。

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