دورية أكاديمية
Jejunal Leiomyosarcoma in a Young Adult: Distinguishing from Gastrointestinal Stromal Tumor through Radiographic, Histologic, and Epidemiologic Analysis - A Case Report.
| العنوان: | Jejunal Leiomyosarcoma in a Young Adult: Distinguishing from Gastrointestinal Stromal Tumor through Radiographic, Histologic, and Epidemiologic Analysis - A Case Report. |
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| المؤلفون: | Bentley BH; Department of Internal Medicine, Wake Forest University School of Medicine, Winston-Salem, NC, USA., Ellington AL; Department of Internal Medicine, Wake Forest University School of Medicine, Winston-Salem, NC, USA., Guo AA; Department of Internal Medicine, Wake Forest University School of Medicine, Winston-Salem, NC, USA., Lu H; Department of Pathology, Wake Forest University School of Medicine, Winston-Salem, NC, USA., Lippert WC; Department of Internal Medicine, Wake Forest University School of Medicine, Winston-Salem, NC, USA. |
| المصدر: | Gastrointestinal tumors [Gastrointest Tumors] 2024 Apr 17; Vol. 10 (1), pp. 38-43. Date of Electronic Publication: 2024 Apr 17 (Print Publication: 2023). |
| نوع المنشور: | Case Reports; Journal Article |
| اللغة: | English |
| بيانات الدورية: | Publisher: S. Karger Medical and Scientific Publishers Country of Publication: Switzerland NLM ID: 101644585 Publication Model: eCollection Cited Medium: Print ISSN: 2296-3774 (Print) Linking ISSN: 22963774 NLM ISO Abbreviation: Gastrointest Tumors Subsets: PubMed not MEDLINE |
| أسماء مطبوعة: | Original Publication: Basel : S. Karger Medical and Scientific Publishers |
| مستخلص: | Introduction: Primary small intestinal malignancies are rare with an incidence of less than 5% of all gastrointestinal malignancies and are more common in the middle-aged and elderly population. They are comprised either an adenocarcinoma, neuroendocrine tumor, gastrointestinal stromal tumor (GIST), lymphoma, and/or sarcoma. Case Presentation: Here we exhibit the case of a 23-year-old who presented with progressive nausea, weight loss, abdominal pain, and iron deficiency anemia and was diagnosed with leiomyosarcoma of the jejunum. Conclusion: We distinguish a GIST from leiomyosarcoma based on radiographic, histologic, and epidemiologic evidence and review the significance of prompt, accurate diagnosis as related to treatment. Competing Interests: The authors have no conflicts of interest to declare. (© 2024 The Author(s). Published by S. Karger AG, Basel.) |
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| فهرسة مساهمة: | Keywords: Case report; GI tumors; Gastrointestinal cancer; Gastrointestinal stromal tumors; Leiomyosarcoma; Smooth muscle tumor; Soft tissue sarcoma; Tumor biomarkers |
| تواريخ الأحداث: | Date Created: 20240717 Latest Revision: 20240718 |
| رمز التحديث: | 20240718 |
| مُعرف محوري في PubMed: | PMC11249453 |
| DOI: | 10.1159/000538430 |
| PMID: | 39015763 |
| قاعدة البيانات: | MEDLINE |
| تدمد: | 2296-3774 |
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| DOI: | 10.1159/000538430 |