scholarly journals A Rare Case of Duodenal Carcinoid Tumors in a Patient With Atypical Symptoms

2020 ◽  
Vol 10 (1-2) ◽  
pp. 7-9
Author(s):  
Tanisha Wandhare ◽  
Manrique Guerrero ◽  
Robert Madlinger ◽  
Jamshed Zuberi

2018 ◽  
Vol 154 (6) ◽  
pp. S-196-S-197
Author(s):  
Nadim Mahmud ◽  
Yutaka Tomizawa ◽  
Kristen M. Stashek ◽  
Bryson W. Katona ◽  
David C. Metz


2009 ◽  
Vol 24 (2) ◽  
pp. 471-475 ◽  
Author(s):  
Hironori Tsujimoto ◽  
Takashi Ichikura ◽  
Shigeaki Nagao ◽  
Tomoki Sato ◽  
Satoshi Ono ◽  
...  


2013 ◽  
Vol 144 (5) ◽  
pp. S-757-S-758
Author(s):  
Hye Yon Park ◽  
Kyung-suk Lim ◽  
Byung-Hoon Min ◽  
Eun Ran Kim ◽  
Jun Haeng Lee ◽  
...  


2019 ◽  
Vol 10 (1) ◽  
pp. 73-75
Author(s):  
Israt Rezwana ◽  
Sourav Sarkar ◽  
Rushda Sharmin Binte Rouf ◽  
Sultana Marufa Shefin ◽  
SM Ashrafuzzaman

Adrenal sarcomatoid carcinoma (ASC) are very rare and aggressive malignant tumors of adrenal glands containing both epithelial (carcinomatous) and mesenchymal (sarcomatous) components. ASC presents a diagnostic challenge due to its atypical symptoms and histological patterns which influence treatment.At the time of diagnosis, a large percentage of patients are already at the metastatic stage and succumb within a few months. Here, we report a case of functional sarcomatoid carcinoma in right adrenal gland in a 37-year-old female, who presented with new onset hypertension. The patient underwent right sided adrenalectomy and she was alive at the time of writing the current report.To the best of our knowledge, ASC reported in literature to date showed only few patient presented with endocrine hypersecretion and only one patient presented with both hypertension and endocrine dysfunction. So, our case is the rarest among the rare. Birdem Med J 2020; 10(1): 73-75



2008 ◽  
Vol 103 ◽  
pp. S299
Author(s):  
Thomas Park ◽  
Kevin Jo ◽  
Ashok Shah ◽  
Asad Ullah


2008 ◽  
Vol 134 (4) ◽  
pp. A-854
Author(s):  
Kenzo Hirose ◽  
Brown Nancy ◽  
Kristina Potanos ◽  
Bipan Chand ◽  
R. Matthew Walsh


2011 ◽  
Vol 73 (4) ◽  
pp. AB449 ◽  
Author(s):  
Bryan L. Balmadrid ◽  
Robert G. Walker ◽  
Paul S. Jowell ◽  
Rebecca Burbridge ◽  
Michael Feiler ◽  
...  


Author(s):  
Snehal G. Murde ◽  
Rohini R. Raut ◽  
Beena Kumari ◽  
Dinesh C. Hojai

Non puerperal uterine inversion is a very rare clinical scenario with very few gynaecologist actually managing it in their lifetime. Acute variety of non-puerperal inversion is even rarer and thus possess diagnostic and management challenges. Case study of a rare case of a 45 years old female who was admitted for an elective surgery and had sudden acute inversion of uterus which was clinically diagnosed. Patient was managed by debulking of tumour which turned out to be large leiomyoma, followed by total abdominal hysterectomy. Rarity of the disease, atypical symptoms and less clinical exposure to such cases pose diagnostic as well as surgical challenges as in our case.



2019 ◽  
Vol 156 (6) ◽  
pp. S-371
Author(s):  
Shria Kumar ◽  
Nadim Mahmud ◽  
Robert E. Roses ◽  
Bryson W. Katona ◽  
Gregory G. Ginsberg ◽  
...  


1999 ◽  
Vol 123 (7) ◽  
pp. 635-637
Author(s):  
Dolores López-Terrada ◽  
M. G. K. Bloom ◽  
Philip T. Cagle ◽  
Mary L. Ostrowski

Abstract We report a rare case of an oncocytic mucoepidermoid carcinoma of the trachea, which presented in a 78-year-old woman with hemoptysis. Oncocytic cells comprised the majority of this low-grade lesion and demonstrated granular cytoplasmic phosphotungstic acid–hematoxylin staining as well as strong immunohistochemical reactivity to antimitochondrial antibody. Most tracheobronchial tumors with oncocytic change are carcinoid tumors. To our knowledge, this is the first oncocytic mucoepidermoid carcinoma of the trachea reported. This diagnosis was facilitated by histochemical and immunohistochemical studies.



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