A Rare Clinical Entity of Krukenberg Tumor: A Case Report in Margono Soekarjo Hospital of Purwokerto

Aditya Eka Octavian, M. Yamsun, Gita Nawangtantrini
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Abstract

Introduction: Krukenberg Tumor is an ovarian tumor that originated from other organ metastases such as gastric, colorectal, pylorus, appendix, colorectal, or breasts. This study aims to report an incidence of a Krukenberg tumor found in a-36year- old woman who has finished her therapy at Margono Soekarjo Hospital.Case Presentation: This case reports the incidence of a Krukenberg tumor found in a-36-year old woman with the main complaint of a burning sensation in her stomach and the existence of a mass in the right and under the Arcus Costae. The patient underwent metastasectomy and biopsy. Histopathological examinations show that the features of Krukenberg tumor originated from a gaster. The patient then underwent chemotherapy for 6 cycles, radiotherapy 20 times, and some evaluation. This case had been observed for 12 months since the first time the patient came to the hospital.Conclusions: Krukenberg tumor is a rare tumor of the ovary which is characterized by poor prognosis. This case depicts the finding of Krukenberg tumor with gastric clinical features. The combination of metastasectomy and chemotherapy can be done in such a case to improve patient survival rates.
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一种罕见的临床肿瘤:普沃克尔托Margono Soekarjo医院一例报告
简介:Krukenberg肿瘤是一种起源于其他器官转移的卵巢肿瘤,如胃、结肠、幽门、阑尾、结肠或乳房。本研究旨在报告一名36岁妇女在Margono Soekarjo医院完成治疗后发现的Krukenberg肿瘤的发生率。病例介绍:本病例报告了一名36岁女性的Krukenberg肿瘤,主要主诉为胃灼烧感,右侧和肋弓下存在肿块。患者接受了转移瘤切除术和活检。组织病理学检查显示,Krukenberg肿瘤的特征起源于胃。化疗6个周期,放疗20次,并进行一些评价。自患者第一次来医院观察12个月。结论:Krukenberg肿瘤是一种罕见的卵巢肿瘤,预后较差。本病例描述了具有胃临床特征的Krukenberg肿瘤的发现。在这种情况下,可以联合进行转移性切除和化疗,以提高患者的生存率。
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