scholarly journals Nodular fasciitis of the face: A case report

2019 ◽  
Vol 61 ◽  
pp. 207-209 ◽  
Author(s):  
Shems Al-Hayder ◽  
Mads Warnecke ◽  
Jørgen Hesselfeldt-Nielsen
Keyword(s):  
Case Report ◽  
Nodular Fasciitis ◽  
The Face

Congenital extraskeletal Ewing's sarcoma of the face: A case report

Head & Neck ◽  
1994 ◽  
Vol 16 (1) ◽  
pp. 75-78 ◽  
Author(s):  
Thiam Chye Lim ◽  
Walter Tiang Lee Tan ◽  
Yoke Sun Lee
Keyword(s):  
Case Report ◽  
Ewing’S Sarcoma ◽  
Ewing's Sarcoma ◽  
The Face ◽  
Extraskeletal Ewing’S Sarcoma

Spindle cell liposarcoma of the face: case report and literature review

2010 ◽  
Vol 163 (3) ◽  
pp. 638-640 ◽  
Author(s):  
T. Agostini ◽  
C. Catelani ◽  
A. Acocella ◽  
A. Franchi ◽  
R. Bertolai ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Spindle Cell ◽  
The Face

Nodular Fasciitis of Neck: A Case Report

2021 ◽  
Vol 11 (02) ◽  
pp. 101-106
Author(s):  
军鹏 张
Keyword(s):  
Case Report ◽  
Nodular Fasciitis

Primary Peritonitis Due to Group G Streptococcus: A Case Report

PEDIATRICS ◽  
1975 ◽  
Vol 56 (6) ◽  
pp. 1078-1079
Author(s):  
Abdul J. Khan ◽  
Hugh E. Evans ◽  
Marylu R. Macabuhay ◽  
Yu-En Lee ◽  
Robert Werner
Keyword(s):  
Case Report ◽  
Burn Injury ◽  
Past History ◽  
Abdominal Distension ◽  
Streptococcus Group ◽  
Primary Peritonitis ◽  
The Face ◽  
Life Threatening ◽  
Average Size ◽  
Streptococcus A

Beta-hemolytic Streptococcus group G, a rare human pathogen, has long been implicated in human disease as causing pharyngitis, puerperal sepsis, empyema, and even septicemia. We are reporting a rare, life-threatening, acute illness, primary peritonitis, due to this organism, whose etiological source probably was a family dog. Case Report R.K., a 2-year-old girl, was admitted with the complaints of anorexia, vomiting of three days' duration, and severe abdominal distension of one day's duration. The symptoms started following a burn injury over the face and lips three days prior to admission. Past history was noncontributory. Physical examination revealed an ill child of average size, fully conscious.

scholarly journals Bilateral Sturge Weber Syndrome- a rare case report

2013 ◽  
Vol 5 (1) ◽  
pp. 129-132 ◽  
Author(s):  
P Singh ◽  
S Singh
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Unusual Case ◽  
The Other ◽  
Advanced Stage ◽  
Weber Syndrome ◽  
Rare Case Report ◽  
The Face ◽  
Bilateral Condition ◽  
Sturge Weber Syndrome

Background: Sturge-Weber syndrome is a rare congenital neuro- oculo- cutaneous disorder. Objective: To report a very rare unusual case of bilateral manifestation of Sturge Weber syndrome. Case: We report an unusual case of a 17-year-old female with advanced stage of bilateral glaucoma associated with facial nevus extending to the other half of the face as well and bilateral intracranial calcification. Conclusion: Sturge -Weber syndrome can manifest as a bilateral condition. Nepal J Ophthalmol 2013; 5(9):129-132 DOI: http://dx.doi.org/10.3126/nepjoph.v5i1.7841

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.

scholarly journals Solitary neurofibroma of the face masquerading as a low-flow vascular malformation – case report and experience of management

JPRAS Open ◽  
2019 ◽  
Vol 19 ◽  
pp. 67-72 ◽  
Author(s):  
Stephen R Ali ◽  
Susan A Hendrickson ◽  
Graham Collin ◽  
Jon Oxley ◽  
Robert P Warr
Keyword(s):  
Case Report ◽  
Vascular Malformation ◽  
Low Flow ◽  
Solitary Neurofibroma ◽  
The Face
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