• 제목/요약/키워드: gastrointestinal stromal tumor

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A Rare Duodenal Subepithelial Tumor: Duodenal Schwannoma

  • Kahng, Dong Hwahn;Kim, Gwang Ha;Park, Sang Gyu;Lee, So Jeong;Park, Do Youn
    • Clinical Endoscopy
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    • 제51권6호
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    • pp.587-590
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    • 2018
  • Schwannomas are uncommon neoplasms that arise from Schwann cells of the neural sheath. Gastrointestinal schwannomas are rare among mesenchymal tumors of the gastrointestinal tract, and only a few cases have been reported to date. Duodenal schwannomas are usually discovered incidentally and achieving a preoperative diagnosis is difficult. Schwannomas can be distinguished from other subepithelial tumors on endoscopic ultrasonography; however, any typical endosonographic features of duodenal schwannomas have not been reported due to the rarity of these tumors. Immunohistochemistry is essential to distinguish schwannomas from gastrointestinal stromal tumors and leiomyomas. We report a case of duodenal schwannoma found incidentally during a health checkup endoscopy. On endoscopic ultrasonography, this tumor was suspected as a gastrointestinal stromal tumor; therefore, the patient underwent laparoscopic wedge resection of the tumor. Histopathology and immunohistochemistry confirmed that the duodenal lesion was a benign schwannoma.

원인불명의 위장관 출혈을 보인 소장 위장관 기질종양 식별: 혈관조영술 소견의 강조 (Identifying Small Bowel Gastrointestinal Stromal Tumor as the Culprit Lesion in Obscure Gastrointestinal Bleeding: Emphasis on Angiographic Findings)

  • 최형인;최민정;김봉만;남궁환;최승규
    • 대한영상의학회지
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    • 제83권2호
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    • pp.400-405
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    • 2022
  • 위장관기질종양(gastrointestinal tumor; 이하 GIST)은 종종 위장관 출혈의 원인이 되는 드물지 않은 질환이지만 소장에 생기는 경우 내시경 및 전산화단층촬영(이하 CT)에서 발견이 어려울 수 있다. 본 증례에서 환자는 수술 전 총 3회의 CT를 시행 받았으나, 병변은 매번 복강의 다른 부위에 위치해 있었고, 허탈된 소장과 구분이 어려워 처음 2번의 CT에서는 발견하지 못했다. 혈관조영술에서 병변이 보였지만, 고령의 환자에서 원인불명 위장관 출혈의 가장 흔한 원인인 혈관기형으로 잘못 해석되어 올바른 진단과 치료가 3년간 지연되었다. 본 증례를 통해, GIST의 정확한 진단 및 치료 전략 수립을 위해 혈관조영술 소견을 강조하고자 한다.

Contrast Enhanced Ultrasonography and CT Features of Gastrointestinal Stromal Tumor in a Dog

  • Saran Chhoey;Soyeon Kim;Kroesna Kang;Sath Keo;Jihye Choi
    • 한국임상수의학회지
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    • 제40권5호
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    • pp.375-381
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    • 2023
  • A large abdominal mass was incidentally found in a 13-year-old mixed-breed dog and was confirmed to be a cecal gastrointestinal stromal tumor (GIST). Contrast-enhanced ultrasound and post-contrast computed tomography (CT) showed mild contrast enhancement of the mass, indicating low blood flow. The tumor origin was determined to be the cecum by identifying the vessels supplying the mass on post-contrast CT. The exophytic growth of the tumor left the cecal lumen intact without obstruction. This report described the CEUS and CT perfusion of the cecal GIST and perfusion evaluation can help diagnose and characterize GISTs in dogs.

Gastrointestinal Stromal Tumor of the Stomach Presenting as Multilobular with Diffuse Calcifications

  • Kim, Sae Hee;Lee, Moon-Soo;Cho, Byung Sun;Park, Joo-Seung;Han, Hyun-Young;Kang, Dong-Wook
    • Journal of Gastric Cancer
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    • 제16권1호
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    • pp.58-62
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    • 2016
  • Gastrointestinal stromal tumors (GISTs) are the most common primary mesenchymal neoplasms of the gastrointestinal tract and usually appear as a well-circumscribed mass. However, it may be difficult to confirm the extent of the disease for some GISTs. A 70-year-old asymptomatic female presented for a regular physical exam. An esophagogastroduodenoscopy showed a 2.0 cm protruding mass on the gastric fundus. Endoscopic ultrasound revealed an ill-defined heterogenous hypoechoic lesion ($3.0{\times}1.5cm$). A computed tomography (CT) scan demonstrated a 4.5 cm multifocal calcified mass at the gastric body as well as at the gastric fundus. Laparoscopic gastric wedge resection was performed according to the extent of multifocal calcifications that are shown on the CT. Intraoperative specimen mammography and intraoperative biopsy might be helpful to obtain a tumor-free margin. Final pathologic diagnosis was an intermediate risk GIST in multilobular form. In patients with diffuse multifocal calcifications in the stomach, the possibility of GIST should be considered.

식도에 발생한 악성 위장관 간질종양 -1예 보고- (Malignant Gastrointestinal Stromal Tumor of the Esophagus - One case report -)

  • 김경화;김민호;구자홍
    • Journal of Chest Surgery
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    • 제36권8호
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    • pp.619-622
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    • 2003
  • 위장관 간질종양(Gastrointestinal stromal turners, GIST)은 매우 드문 질환이다. 대개 위나 소장에서 발생하는 것으로 되어 있으나, 식도에서의 생기는 경우는 흔하지 않다. 위장관 간질종양은 위장관에서 발생하며 다양한 형태학적 소견을 보일 수 있으며, 기원이 분명치 않은 종양으로 알려져 왔다 저자들은 66세 여자의 하부 식도에서 발생한 악성 위장관 간질종양 1예를 경험하였기에 문헌 고찰과 함께 보고하고자 한다.

위에 동시성으로 발생한 조기위암 및 위장관간질종양 (Synchronous Occurrence of a Gastric Adenocarcinoma and a GIST (Gastrointestinal Stromal Tumor): A Case Report)

  • 지성배;서경진;허훈;전해명
    • Journal of Gastric Cancer
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    • 제7권4호
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    • pp.261-264
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    • 2007
  • 전 세계적으로 위선암은 두 번째로 많은 암 사망의 원인을 차지하며 지역에 따라 유병률의 차이를 보인다. 한편 위장관 간질종양은 다양한 악성도를 갖는 드문 질환이다. 지금까지의 연구결과에 따르면 이 두 종양은 서로 상이한 발병기전을 가지고 있는 것으로 생각되며, 두 종양이 한 환자에서 동시성으로 발병하는 경우는 매우 드물다. 환자는 64세 남자로, 우연히 발견된 위의 종괴 및 궤양 병변으로 본원에 의뢰되었다. 수술 전 검사를 시행한 뒤 위전절제술을 시행하였고, 9 cm 크기의 위장관 간질종양 및 유문부의 조기위암이 동시에 존재하고 있는 것으로 확인되었다. 이러한 현상은 드물지만 위선암의 유병률이 높은 지역에서는 일어날 수 있는 일일 것으로 생각되며, 지금까지 보고된 문헌들에 대한 고찰과 함께 보고하는 바이다.

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Gastrointestinal Stromal Tumors: A Clinicopathologic and Risk Stratification Study of 255 Cases from Pakistan and Review of Literature

  • Din, Nasir Ud;Ahmad, Zubair;Arshad, Huma;Idrees, Romana;Kayani, Naila
    • Asian Pacific Journal of Cancer Prevention
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    • 제16권12호
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    • pp.4873-4880
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    • 2015
  • Purpose: To describe the clinicopathological features of gastrointestinal stromal tumors (GIST) diagnosed in our section and to perform risk stratification of our cases by assigning them to specific risk categories and groups for disease progression based on proposals by Fletcher et al and Miettinen and Lasota. Materials and Results: We retrieved 255 cases of GIST diagnosed between 2003 and 2014. Over 59% were male. The age range was 16 to 83 years with a mean of 51 years. Over 70% occurred between 40 and 70 years of age. Average diameter of tumors was 10 cms. The stomach was the most common site accounting for about 40%. EGISTs constituted about 16%. On histologic examination, spindle cell morphology was seen in almost of 85% cases. CD117 was the most useful immunohistochemical antibody, positive in 98%. Risk stratification was possible for 220 cases. Based on Fletcher's consensus proposal, 62.3 gastric, 81.8% duodenal, 68% small intestinal, 72% colorectal and 89% EGISTs were assigned to the high risk category; while based on Miettinen and Lasota's algorithm, about 48% gastric, 100% duodenal, 76% small intestinal, 100% colorectal and 100% EGISTs in our study were associated with high risk for disease progression, tumor metastasis and tumor related death. Follow up was available in 95 patients; 26 were dead and 69 alive at follow up. Most of the patients who died had high risk disease and on average death occurred just a few months to a maximum of one to two years after initial surgical resection. Conclusions: Epidemiological and morphologic findings in our study were similar to international published data. The majority of cases in our study belonged to the high risk category.

전이성 위장관 기질종양의 수술 후 완치 (Postoperative Cure for Metastatic Gastrointestinal Stromal Tumor)

  • 박은혜;김진일;정대영;박수헌
    • 대한상부위장관⦁헬리코박터학회지
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    • 제18권4호
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    • pp.264-270
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    • 2018
  • Gastrointestinal stromal tumor (GIST) is a mesenchymal tumor derived from Cajal cells originating from the myotonic plexus. The expression of tyrosine kinase (KIT) membrane receptors that are active on KIT is inhibited by the KIT inhibitor imatinib mesylate. GISTs are resistant to conventional chemotherapy, and radiation therapy is not significantly beneficial for GISTs. With the development of imatinib mesylate, approximately 81.6% of patients with advanced and metastatic GIST exhibit an effect above the stabilization response, thereby increasing the survival time. However, imatinib mesylate alone is unlikely to cure metastatic GISTs. Even with a partial or stable response, imatinib mesylate may be used for a longer time period. However, resection of grossly visible lesions should be considered for patients with a stable response during surgical treatment. In this study, we present a case of GIST with liver metastasis after imatinib mesylate treatment, which was followed up without recurrence after partial resection.

Imatinib-induced hepatitis treated by corticosteroids in a patient with metastatic gastrointestinal stromal tumor

  • Kang, Min Kyu;Lee, Heon Ju;Choi, Joon Hyuk
    • Journal of Yeungnam Medical Science
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    • 제36권2호
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    • pp.155-158
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    • 2019
  • Imatinib mesylate is currently used as the first-line treatment for metastatic gastrointestinal stromal tumors (GISTs). Imatinib-induced hepatotoxicity in patients with GIST is very rare. Its features vary from subclinical elevation of serum aminotransferase to clinically apparent acute hepatitis, which is associated with immunologic reactions. Imatinib-induced hepatotoxicity with autoimmune-like features can be treated by the discontinuation of imatinib mesylate and the administration of oral steroids. Here, we report a case of late-onset imatinib-induced hepatitis with autoimmune-like features in a patient with metastatic GIST, which was improved by oral corticosteroids.

위장관기질종양 (Gastrointestinal Stromal Tumors: Case Report, Aeromedical Assessment of Therapy)

  • 전종득
    • 항공우주의학회지
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    • 제30권2호
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    • pp.80-82
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    • 2020
  • Gastrointestinal Stromal Tumors (GISTs) are relatively uncommon soft tissue sarcomas that can be located in any part of the digestive system. GISTs originate in specialized nerve cells located in the walls of the digestive system. This case report is about a 53-year-old airman who was recently diagnosed as peritoneal GISTs. He got a surgical removal of the tumor and chemotherapy, including imatinib (Gleevec®). Although his GISTs have shown excellent clinical progress, he still needs ongoing treatment. This case involves an airline pilot applicant for Class-I medical certification who has had GISTs under chemotherapy.