Bullosis Diabeticorum in a Young Child: Case Report of a Very Rare Entity and a Literature Review

2017 ◽  
Vol 41 (2) ◽  
pp. 129-131 ◽  
Author(s):  
Anca Chiriac ◽  
Irina Costache ◽  
Cristian Podoleanu ◽  
Adrian Naznean ◽  
Simona Stolnicu
Keyword(s):  
Case Report ◽  
Young Child ◽  
Literature Review ◽  
Rare Entity ◽  
Bullosis Diabeticorum

Hemobilia a Rare Entity: Case Report and Literature Review

2016 ◽  
Vol 04 (04) ◽  
Author(s):  
Richard Beaumont ◽  
Iris Garcia ◽  
Marie Josee Valladares
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Rare Entity

scholarly journals Intraosseous Hemangioma of the Middle Turbinate: A Case Report of a Rare Entity and Literature Review

2015 ◽  
Vol 28 (2) ◽  
pp. 148-151 ◽  
Author(s):  
Ryan Goff ◽  
Steven Weindling ◽  
Vivek Gupta ◽  
Aziza Nassar
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Middle Turbinate ◽  
Rare Entity ◽  
Intraosseous Hemangioma

scholarly journals Renal immature teratoma: A rare entity; A case report and literature review

2021 ◽  
Vol 34 ◽  
pp. 101495
Author(s):  
Yonas Girma Shumiye ◽  
Fatuma Yassin Bushra ◽  
Elizabeth Hailemelekot Sirak ◽  
Muluken Bekele Wondimagegnehu
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Immature Teratoma ◽  
Rare Entity

Rectal blue nevus: Case report of a rare entity and literature review

2015 ◽  
Vol 211 (8) ◽  
pp. 625-627 ◽  
Author(s):  
Jasbir Makker ◽  
Sailaja Sakam ◽  
Prasanthi Arety ◽  
Masooma Niazi ◽  
Bhavna Balar
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Rare Entity ◽  
Blue Nevus

Vaginal Leiomyoma: Case Report and Literature Review

2017 ◽  
Vol 5 (1) ◽  
pp. 62-65
Author(s):  
Mamta Gupta ◽  
Rita Jindal ◽  
Supriya Kumari ◽  
Namrata Nargotra
Keyword(s):  
Case Report ◽  
Literature Review ◽  
South Asian ◽  
Coming Out ◽  
Rare Entity ◽  
Review Of Literature ◽  
Vaginal Route ◽  
The Right ◽  
Vaginal Leiomyoma

ABSTRACT Introduction Leiomyoma arising from the vagina is a rare entity with varied presentations. Case Report A woman 44 years of age presented with complaints of something coming out vaginally, polymenorrhea, and pain in abdomen. A mass arising from the right posterolateral wall of vagina was seen. Ultrasound reported it to be cervical fibroid. The mass was enucleated through vaginal route. Histopathology confirmed it to be a leiomyoma. Review of literature revealed that it has a varied presentation. Diagnosis is often missed. Conclusion The condition should always be kept in mind whenever coming across any mass in vagina. How to cite this article Gupta M, Saini V, Jindal R, Kumari S, Nargotra N. Vaginal Leiomyoma: Case Report and Literature Review. J South Asian Feder Menopause Soc 2017;5(1):62-65.

scholarly journals Primary malignant mucosal melanoma of the larynx: A case report and literature review

2015 ◽  
Vol 5 (10) ◽  
pp. 872-874
Author(s):  
S Shrestha Khadka ◽  
MC Lee ◽  
AB Karki
Keyword(s):  
Case Report ◽  
Adjuvant Chemotherapy ◽  
Malignant Melanoma ◽  
Literature Review ◽  
Head And Neck ◽  
Radical Surgery ◽  
Mucosal Melanoma ◽  
Rare Entity ◽  
Mucous Membranes ◽  
Female Genital

Malignant mucosal melanoma is very rare entity. It comprises about 1% of all malignant melanoma and exhibit more aggressive behaviour than that of skin melanomas. Mucosal melanoma arises mainly from the mucous membranes of head and neck, the female genital organs or the anorectal and the urinary tracts.  Laryngeal malignant melanoma constitutes 3.8% to 7.4% of all cases of malignant mucosal melanoma of head and neck. In this article we report a case of primary malignant mucosal melanoma of larynx in 27 years old male who was treated with radical surgery and adjuvant chemotherapy in BPKM Cancer Hospital, Chitwan.

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