Presentación polipoide de un carcinosarcoma primario de vagina. Un caso clinicopatológico de esta neoplasia excepcional

IF 0.1 Q4 OBSTETRICS & GYNECOLOGY
R. Sarabia Ochoa , J.P. García de la Torre , A. Amezcua Recover
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Abstract

Introduction

Gynecological carcinosarcoma, also called malignant mixed Müllerian tumor, is a rare, heterogeneous, aggressive, malignant neoplasm. The vagina as a primary site of carcinosarcoma is exceptional.

Main symptoms and/or clinical findings

95-year-old woman who consulted for vaginal bleeding. The gynecological examination revealed a polypoid tumor dependent on the right lateral wall of the vagina.

Main diagnoses, therapeutic interventions and results The CT radiological study identified a tumor measuring 6 × 3,4 × 3,5 cm, which occupied the lower third of the vagina. The polypoid mass was excised in fragments, with resection of its base in the right medial 1/3 of the vagina. The histological study corresponded to a malignant spindle-cell neoplasm with areas of high cell density, intersecting fascicles and multiple edematous areas, with spindle-shaped or stellate-shaped cells with intense nuclear atypia and monstrous bizarre cells. Chondroid-like or myxoid appearance foci, frequent atypical multinucleated giant tumor cells, mitosis and some foci with evident epithelial differentiation in the form of poorly differentiated carcinoma were observed. The diagnosis was carcinosarcoma. Considering the patient's age, it was decided to perform follow-up without further interventions. Currently, one year after diagnosis, the patient has no evidence of recurrence.

Conclusion

Primary malignant neoplasms of the vagina are very rare. Vaginal carcinosarcoma is an extremely rare neoplasm that occurs in elderly women. The prognosis is poor and more studies are needed to better understand this neoplasm.

阴道原发性癌肉瘤的息肉状表现。这种特殊肿瘤的临床病理病例。
导言妇科癌肉瘤又称恶性混合缪勒氏瘤,是一种罕见的、异质性、侵袭性恶性肿瘤。主要症状和/或临床发现95 岁的女性因阴道出血就诊。妇科检查发现,阴道右侧壁有一个息肉状肿瘤。主要诊断、治疗措施和结果 CT 放射学检查发现,肿瘤大小为 6 × 3.4 × 3.5 厘米,占据了阴道下三分之一处。息肉状肿块被分割切除,其底部位于阴道右内侧 1/3 处。组织学研究显示,这是一种恶性纺锤形细胞肿瘤,细胞密度高,呈束状交错,有多个水肿区,细胞呈纺锤形或星状,核严重不典型,细胞畸形怪异。病灶呈软骨样或肌样外观,常有不典型多核巨型瘤细胞,有丝分裂,部分病灶有明显的上皮分化,呈分化不良癌。诊断结果为癌肉瘤。考虑到患者的年龄,决定对其进行随访,不做进一步干预。结论阴道原发性恶性肿瘤非常罕见。阴道癌肉瘤是一种极为罕见的肿瘤,好发于老年妇女。预后较差,需要进行更多的研究来更好地了解这种肿瘤。
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来源期刊
CiteScore
0.20
自引率
0.00%
发文量
54
期刊介绍: Una excelente publicación para mantenerse al día en los temas de máximo interés de la ginecología de vanguardia. Resulta idónea tanto para el especialista en ginecología, como en obstetricia o en pediatría, y está presente en los más prestigiosos índices de referencia en medicina.
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