Undiagnosed primary lung carcinoma with initial manifestation of small intestinal rupture: A rare case report

2018 ◽  
Author(s):  
Sofia Mavropoulou ◽  
Zoi Tatsiou
Keyword(s):  
Case Report ◽  
Lung Carcinoma ◽  
Rare Case ◽  
Initial Manifestation ◽  
Primary Lung Carcinoma ◽  
Rare Case Report ◽  
Small Intestinal

scholarly journals AGGRESSIVE MESENTRIC FIBROMATOSIS: A RARE CASE REPORT AND REVIEW OF LITERATURE

2013 ◽  
Vol 03 (01) ◽  
pp. 79-82
Author(s):  
Rohan Shetty ◽  
Shubha Bhat ◽  
Rajesh Ballal ◽  
Pramod Makannavar ◽  
Anil Kumar K. N.
Keyword(s):  
Case Report ◽  
Male Patient ◽  
Rare Case ◽  
Clinical Presentation ◽  
Aggressive Fibromatosis ◽  
Definitive Diagnosis ◽  
Review Of Literature ◽  
Therapeutic Challenge ◽  
Rare Case Report ◽  
Small Intestinal

AbstractMesentric fibromatosis is a proliferative fibroblastic neoplasm of the small intestinal mesentery with varied clinical presentation. Giant mesentric fibromatosis is uncommon and its rarity poses a diagnostic and therapeutic challenge. This paper presents a recurrent aggressive fibromatosis in a 38 year old male patient, who had initially undergone a laparotomy outside for mass abdomen but only pus was evacuated and definitive diagnosis was not made.

scholarly journals Ball in the Wall: Mesenteric Fibromatosis—a Rare Case Report

2020 ◽  
Vol 11 (S1) ◽  
pp. 73-77
Author(s):  
Abhinav Deshpande ◽  
Ankita Tamhane ◽  
Y. S. Deshpande ◽  
Radhika Pagey ◽  
Meena Pangarkar
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Desmoid Tumor ◽  
Rare Case ◽  
Soft Tissue Tumor ◽  
Rare Tumor ◽  
Mesenteric Fibromatosis ◽  
Rare Case Report ◽  
Benign Soft Tissue Tumor ◽  
Small Intestinal

Abstract Introduction Mesenteric fibromatosis-desmoid tumor of mesentery is a rare benign soft tissue tumor of mesentery. On CT, it mimics gastrointestinal stromal tumor (GIST). Case Report A 44-year-old female with small intestinal mass, preoperatively diagnosed radiologically and pathologically as GIST. Conclusion Mesenteric fibromatosis is a rare tumor often mistaken for GIST. Histopathology and immunohistochemistry is the key as management of both the tumors differs.

scholarly journals A rare case report of bilateral testicular masses as an initial manifestation of systemic sarcoidosis

2015 ◽  
Vol 0 (0) ◽  
pp. 0
Author(s):  
Hamid Shaaban ◽  
Abhishek Kumar ◽  
Tejas Modi ◽  
Michael Maroules ◽  
Hiren Patel
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Initial Manifestation ◽  
Rare Case Report ◽  
Systemic Sarcoidosis

Primary neuroendocrine carcinoma of renal: a rare case report

2014 ◽  
Author(s):  
Tadeusz Budlewski ◽  
Dorota Szydlarska ◽  
Norbert Szalus ◽  
Jolanta Kijek ◽  
Beata Ewa Chrapko
Keyword(s):  
Case Report ◽  
Neuroendocrine Carcinoma ◽  
Rare Case ◽  
Rare Case Report

Combination of turner syndrome and congenital adrenal hyperplasia: a rare case report

2017 ◽  
Author(s):  
Ivana Sagova ◽  
Dušan Pavai ◽  
Matej Stančik ◽  
Helena Urbankova ◽  
Juliana Gregova ◽  
...  
Keyword(s):  
Case Report ◽  
Congenital Adrenal Hyperplasia ◽  
Turner Syndrome ◽  
Rare Case ◽  
Adrenal Hyperplasia ◽  
Rare Case Report
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