scholarly journals Massive hemoptysis: A rare case with uncommon presentation and rapid response – A case report

2020 ◽  
Vol 31 ◽  
pp. 101144
Author(s):  
Vishak Acharya ◽  
A. Shreenivasa ◽  
Deepa Adiga ◽  
Chakrapani Mahabala ◽  
Sajjan Shenoy ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Rapid Response ◽  
Massive Hemoptysis ◽  
Uncommon Presentation

scholarly journals Giant hamartoma of lung presented with massive hemoptysis: A rare case report and review of the literature

Rare Tumors ◽  
2019 ◽  
Vol 11 ◽  
pp. 203636131882392 ◽  
Author(s):  
Bita Geramizadeh ◽  
Maedeh Mottavvas ◽  
Bijan Zeyaian ◽  
Armin Amirian
Keyword(s):  
Case Report ◽  
Chest Radiography ◽  
Rare Case ◽  
English Literature ◽  
Massive Hemoptysis ◽  
Review Of The Literature ◽  
Uncommon Presentation ◽  
Plain Chest ◽  
Rare Case Report ◽  
Pulmonary Hamartoma

Hamartoma of lung is a common tumor, majority of which are small and incidentally discovered during plain chest radiography. Our case is a 30-year-old gentleman with an extremely uncommon presentation of a common tumor, that is, a giant hamartoma of lung presenting as massive hemoptysis and intractable cough. To the best of our knowledge, such occurrence of giant pulmonary hamartoma is very uncommon and its presentation with massive hemoptysis is even more uncommon. Less than 20 cases of giant hamartoma of lung have been reported in the English literature so far.

An Uncommon Presentation of Polycythemia Vera as Ischemic Stroke—A Rare Case Report

2012 ◽  
Vol 3 (5) ◽  
pp. 455-457
Author(s):  
Dr .KOUSHIK GUDAVALLI ◽  
◽  
Dr .SHILPA CHIKATI ◽  
Dr .MOHAN RAO JAKKAMPUTI ◽  
Dr .KAMAL LOCHAN BEHERA ◽  
...  
Keyword(s):  
Ischemic Stroke ◽  
Case Report ◽  
Polycythemia Vera ◽  
Rare Case ◽  
Uncommon Presentation ◽  
Rare Case Report

Rare case of perforated appendicitis presenting as persistent perineal discharge following laparoscopic abdominoperinal excision of rectum (APER)

2021 ◽  
Vol 14 (1) ◽  
pp. e236312
Author(s):  
Tanmoy Mukherjee ◽  
Shantata Jayant Kudchadkar ◽  
Jayesh Sagar ◽  
Shashank Gurjar
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Perforated Appendicitis ◽  
Perineal Wound ◽  
Abdominoperineal Excision ◽  
Major Surgery ◽  
Salvage Procedure ◽  
Uncommon Presentation ◽  
Rare Case Report ◽  
History Of

Abdominoperineal excision of rectum (APER) is one of the widely used surgical procedures to treat low rectal cancer, benign conditions like Crohn’s proctitis with anal involvement and as a salvage procedure for anal cancer. Perineal wound infection is a well-recognised complication following such major surgery. Occurrence of appendicitis in a few weeks’ time following such a major surgery is uncommon. However, here we present a rare case report of perforated appendicitis presenting as persistent perineal discharge in an elderly man, following laparoscopic APER for a low rectal tumour. To our knowledge, this is the first time such a rare clinical presentation of appendicitis is reported in the history of medical literature. Through this case report, we aim to highlight the importance of considering such an uncommon presentation in patients with perineal discharge, following APER.

scholarly journals Uncommon plasmacytoid myoepithelioma originating from ectopic minor salivary gland in neck: a rare case with rare site presentation

2020 ◽  
Vol 8 (9) ◽  
pp. 3367
Author(s):  
Nidhi Verma ◽  
Preeti Singh ◽  
Amod Kumar Saroj ◽  
Priya Gupta
Keyword(s):  
Salivary Gland ◽  
Case Report ◽  
Lymph Node ◽  
Cervical Lymph Node ◽  
Rare Case ◽  
Minor Salivary Gland ◽  
Cervical Region ◽  
Major Salivary Gland ◽  
Uncommon Presentation ◽  
Rare Site

The aim of this case report is to present as case of plasmacytoid at ectopic minor salivary gland in the neck which is a rare neoplasm with uncommon presentation of site. Usually it is a tumor of major salivary gland and more common in parotid gland and less common in the minor salivary gland of the oral cavity predominantly in palate. Here authors are discussing a case of 10-year-old female who presented in our institute with complain of swelling over right mid cervical region which was clinically suspected as reactive cervical lymph node. Patient was evaluated further and cytologically diagnosed as a case of plasmacytoid myoepithelioma. It was also confirmed as a case of plasmacytoid myoepithelioma after histopathology and immunohistochemistry studies. Plasmacytoid myoepithelioma at ectopic minor salivary gland site in the neck is uncommon presentation and only a limited number of cases have been reported in literature.

scholarly journals Unusual site and uncommon presentation of epidermoid cyst: a rare case report and review of literature

2013 ◽  
Vol 2013 (jan08 1) ◽  
pp. bcr2012007907-bcr2012007907 ◽  
Author(s):  
M. R. Sahoo ◽  
M. S. Gowda ◽  
S. S. Behera
Keyword(s):  
Case Report ◽  
Epidermoid Cyst ◽  
Rare Case ◽  
Review Of Literature ◽  
Unusual Site ◽  
Uncommon Presentation ◽  
Rare Case Report

scholarly journals Ruptured Primary Ovarian Pregnancy: A Rare Case Report

2013 ◽  
Vol 10 (3) ◽  
pp. 76-77 ◽  
Author(s):  
Abha Shrestha ◽  
CD Chawla ◽  
RM Shrestha
Keyword(s):  
Medical Journal ◽  
Case Report ◽  
Ovarian Cyst ◽  
Rare Case ◽  
First Trimester ◽  
Tubal Ectopic Pregnancy ◽  
Ovarian Pregnancy ◽  
Ectopic Gestation ◽  
Uncommon Presentation ◽  
Rare Case Report

Ovarian pregnancy is an uncommon presentation of ectopic gestation and usually, it ends with rupture before the end of the first trimester. Its presentation often is difficult to distinguish from that of tubal ectopic pregnancy and hemorrhagic ovarian cyst. We report a rare primary ruptured ovarian pregnancy in a 26 years lady. Kathmandu University Medical Journal | VOL.10 | NO. 3 | ISSUE 39 | JUL- SEP 2012 | Page 76-77 DOI: http://dx.doi.org/10.3126/kumj.v10i3.8026

scholarly journals UNCOMMON PRESENTATION OF UNNOTICED EMBEDDED FOREIGN BODY NECK : A RARE CASE REPORT

2015 ◽  
Vol 4 (33) ◽  
pp. 5783-5786
Author(s):  
Parusharam N ◽  
Ashok Reddy K ◽  
Hanumantha Rao A V S ◽  
Jadi Lingaiah
Keyword(s):  
Case Report ◽  
Foreign Body ◽  
Rare Case ◽  
Uncommon Presentation ◽  
Rare Case Report

Large Vulvar Lipoma in an Adolescent: A Case Report

JMS SKIMS ◽  
2011 ◽  
Vol 14 (1) ◽  
pp. 28-29
Author(s):  
R K Maurya ◽  
Pawan Kumar Singh ◽  
Sandeep Singh
Keyword(s):  
Case Report ◽  
Epithelial Cell ◽  
Adolescent Girl ◽  
Rare Case ◽  
Mesenchymal Cell ◽  
Benign Tumors ◽  
Melanocytic Tumors

Lipomas of vulva have been reported only rarely. Benign tumors of the vulva are normally classified according to their origin as epithelial cell tumors (e.g., keratinocytic, adnexal and ectopic tumors), or mesenchymal cell tumors (e.g., vascular, fibrous, muscular, neural, adipose and melanocytic tumors). Vulvar lipomas need to be differentiated from liposarcomas, which are rare but are very similar to lipomas clinically. Here we present a rare case of large vulvar lipoma in an adolescent girl. JMS 2011;14(1):28-29

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
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