• Tidak ada hasil yang ditemukan

Synchronous Gastrointestinal Stromal Tumor (GIST) with pancreatic adenocarcinoma: A case report

N/A
N/A
Protected

Academic year: 2024

Membagikan "Synchronous Gastrointestinal Stromal Tumor (GIST) with pancreatic adenocarcinoma: A case report"

Copied!
1
0
0

Teks penuh

(1)

Synchronous Gastrointestinal Stromal Tumor (GIST) with pancreatic adenocarcinoma: A case report

ABSTRACT

Introduction: Gastrointestinal Stromal Tumors (GIST) are rare mesenchymal neoplasm of gastrointestinal tract. Stomach is the most common site affected by GIST compared to other places in gastrointestinal track. The coexistence of GIST with another malignancy represents a rare phenomenon with few literature reported. Case presentation: We present here 65 years old patient with stomach GIST and synchronous pancreatic adenocarcionoma discovered during surgery for suspected pancreatic mucinious cystadenoma. Distal pancreaticosplenectomy with excision of GIST Tumor & wedge resection of stomach was done.

Histopathological examination of resected specimens reported the margins are clear.

Discussion: In this article we discuss on the option of systemic therapy versus upfront surgery and their outcome benefit based on literature review. Conclusion: The coexistence of GIST with pancreatic adenocarcinoma is a rare condition. High clinical analysis needed during laparotomy for GIST to detect a synchronous tumor. In a case of GIST the surgeon should recognize the possibility of another tumor with different histological origin. Surgical excision is the mainstay of therapy and it has proven to be curative for our patient. . Due to its rare occurrence and limited literature further studies has to be done on GIST with other synchronous tumor to help the surgeon to manage the patient optimally.

Referensi

Dokumen terkait

Basal Cell Carcinoma and Thyroid Tumor ( Two Primary Tumors ) in Female 74 Years Old : A Case Report.. I Kt Wisudana Yuana 1, IB Made Suryawisesa, Pt Anda Tusta A, Gede

We report a case of a female adult presenting with unilateral Wilms tumor who underwent primary surgical excision and subsequent chemotherapy for

A clinically silent tumour of adrenal myelolipoma: A case report ABSTRACT INTRODUCTION: Adrenal myelolipoma is a rare, non-functional, benign neoplasm which is constituted of mature

Schwannoma of the vagus nerve, a rare middle mediastinal neurogenic tumor: case report.. Das A, Choudhury S, Basuthakur S, Mukhopadhyay A, Mukherjee

Keywords: Adult; Desmoplastic small round cell tumor; Intra-abdominal Introduction Intra-abdominal Desmoplastic small round cell tumor IADSRCT, a distinct and rare entity among the

perivascular epithelioid cells Tumor, PECOMA, HMB45, Angiomyolipoma INTRODUCTION Epithelioid mesenchymal tumors of the uterus were previously considered to be either from smooth

Master of mimicry: Rare primary cutaneous anaplastic large cell lymphoma presenting as fungating parotid tumor–case report and review ABSTRACT Introduction Primary cutaneous

CASE PRESENTATION: We report a patient with multiple glomus tumors on the time of diagnosis, which was histologically diagnosed as an atypical glomus tumor following resection of a