A Rare Location : A Giant Mesenteric Lipoma

2016 ◽  
Vol 24 (1) ◽  
pp. 24-26
Author(s):  
Mehmet Ozer ◽  
Serap Ulusoy ◽  
Omer Parlak
Keyword(s):  
Rare Location ◽  
Mesenteric Lipoma

scholarly journals A Rare Location: A Giant Mesenteric Lipoma

2016 ◽  
Vol 24 (1) ◽  
pp. 24-26
Author(s):  
Mehmet Özer ◽  
Serap Ulusoy ◽  
Ömer Parlak
Keyword(s):  
Rare Location ◽  
Mesenteric Lipoma

Atypical lipomatous tumour of the breast – reporting a not-so-rare entity in an extraordinarily rare location

2018 ◽  
Author(s):  
Simona-Alina Barbu ◽  
Antonia-Carmen Lisievici ◽  
Tiberiu Augustin Georgescu ◽  
Maria Sajin
Keyword(s):  
Rare Entity ◽  
Lipomatous Tumour ◽  
Rare Location

scholarly journals Chondrosarcoma of the parapharyngeal space: Case report and literature review of an extremely rare location

2021 ◽  
Vol 16 (5) ◽  
pp. 1099-1102
Author(s):  
Meryeme Chihabeddine ◽  
Asmaa Naim ◽  
Mariam Kassimi ◽  
Jihane Habi ◽  
Mohamed Mahi ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Parapharyngeal Space ◽  
Rare Location ◽  
Space Case

scholarly journals Intraventricular brain mass causing obstructive hydrocephalus: A rare location of prostate cancer metastasis

2021 ◽  
Vol 23 ◽  
pp. 101024
Author(s):  
William Richardson ◽  
Praveen Satarasinghe ◽  
Min Wang ◽  
James Rose ◽  
Ramsey Ashour
Keyword(s):  
Prostate Cancer ◽  
Cancer Metastasis ◽  
Obstructive Hydrocephalus ◽  
Brain Mass ◽  
Prostate Cancer Metastasis ◽  
Rare Location

scholarly journals Endoscopic Surgery of Congenital Cholesteatoma in the Anterior Epitympanic Recess: A Case Report of a Rare Location

2020 ◽  
pp. 014556132096924
Author(s):  
Hong Chan Kim ◽  
Hyung Chae Yang ◽  
Hyong-Ho Cho
Keyword(s):  
Case Report ◽  
Minimally Invasive ◽  
Middle Ear ◽  
Endoscopic Surgery ◽  
Minimally Invasive Approach ◽  
Ear Surgery ◽  
Invasive Approach ◽  
Congenital Cholesteatoma ◽  
Rare Location ◽  
Histopathological Type

Congenital cholesteatoma is a whitish mass in the middle ear medial to an intact tympanic membrane. It is often without symptoms and therefore incidentally diagnosed. Pediatric congenital cholesteatoma generally starts as a small pearl-like mass in the middle ear cavity that eventually expands to involve the ossicles, epitympanum, and mastoid. The location, size, histopathological type, and extent of the mass must be evaluated to select the appropriate surgical method. Although microscopic ear surgery has traditionally been performed to remove congenital cholesteatoma, a recently introduced alternative is endoscopic surgery, which allows a minimally invasive approach and has better visualization. Here, we report the first known case of a patient with congenital cholesteatoma in the anterior epitympanic recess and discuss the utility of an endoscopic approach in the removal of a congenital cholesteatoma in the hidden area within the middle ear.

scholarly journals Optic pathway gliosarcoma: A very rare location for a rare disease

2021 ◽  
Vol 16 (7) ◽  
pp. 1665-1668
Author(s):  
Renato Masson de Almeida Prado ◽  
Bruno Pierri Tamura ◽  
Gustavo Dalul Gomez
Keyword(s):  
Rare Disease ◽  
Optic Pathway ◽  
Rare Location

Primary axillary hydatid cyst: A rare location

2021 ◽  
Vol 99 (6) ◽  
pp. 466
Author(s):  
Ali Bilal Ulas ◽  
Hayri Ogul ◽  
Yener Aydin ◽  
Atila Eroglu
Keyword(s):  
Hydatid Cyst ◽  
Rare Location

Solitary Fibrous Tumor of the Sella Mimicking Pituitary Adenoma: An Uncommon Tumor in a Rare Location—A Case Report

2009 ◽  
Vol 20 (1) ◽  
pp. 56-61 ◽  
Author(s):  
Tania Weber Furlanetto ◽  
Cláudio Faria Pitta Pinheiro ◽  
Paulo Petry Oppitz ◽  
Luiz Carlos de Alencastro ◽  
Sylvia L. Asa
Keyword(s):  
Case Report ◽  
Pituitary Adenoma ◽  
Solitary Fibrous Tumor ◽  
Rare Location ◽  
Fibrous Tumor ◽  
Uncommon Tumor

scholarly journals Primary Mesenteric Lipoma Causing Closed Loop Bowel Obstruction: A Case Report

2005 ◽  
Vol 21 (3) ◽  
pp. 138-141 ◽  
Author(s):  
Heong-Ieng Wong ◽  
Chiao-Yun Chen ◽  
Gin-Chung Liu
Keyword(s):  
Case Report ◽  
Bowel Obstruction ◽  
Closed Loop ◽  
Mesenteric Lipoma

scholarly journals Nodular fasciitis on the zygomatic region: a rare presentation

2013 ◽  
Vol 88 (6 suppl 1) ◽  
pp. 89-92 ◽  
Author(s):  
Ilner de Souza e Souza ◽  
Mayra Carriijo Rochael ◽  
Rogério Estevam Farias ◽  
Roberto Bezerra Vieira ◽  
Janaina Silva Tirapelle Vieira ◽  
...  
Keyword(s):  
Benign Tumor ◽  
Histopathological Examination ◽  
Excisional Biopsy ◽  
Nodular Fasciitis ◽  
Rare Presentation ◽  
Ki 67 ◽  
Immunohistochemical Markers ◽  
The Face ◽  
Rare Location ◽  
High Cellularity

Nodular fasciitis is a benign tumor, resulting from reactive proliferation composed of fibroblastic/myofibroblastic cells. Due to its rapid growth and high cellularity it may be mistaken for sarcoma. Despite the possibility of spontaneous regression, excision is the treatment of choice. A 24-year-old female patient presented with a nodule on the zygomatic region with 3 months of evolution. Excisional biopsy was performed. Histopathological examination associated with immunohistochemical markers HHF35, AML and Ki-67 allowed diagnostic confirmation. The main relevance of the case presented is its rare location, suggesting its inclusion among the differential diagnoses of tumor lesions on the face.

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