scholarly journals Mandibular neurofibroma: Case report of a rare tumor

2019 ◽  
Vol 9 (4) ◽  
Author(s):  
Ziad Sleiman ◽  
Loubna Abboud ◽  
Elie Mehanna ◽  
Ramzi Mahmoud ◽  
Elie Yaacoub ◽  
...  
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Surgical Management ◽  
Rare Tumor ◽  
Review Of The Literature ◽  
Histological Features ◽  
Jaw Bone

Neural tumors localized in jaw bone are relatively rare. This article presents a case of intraosseous neurofibroma of the mandible in a 37-year-old female patient. A review of clinical, radiographic, histological features and surgical management of the patient are discussed along with a review of the literature.

Ectrodactyly-ectodermal dysplasia-clefting syndrome

2000 ◽  
Vol 90 (9) ◽  
pp. 460-464 ◽  
Author(s):  
GJ Kelman ◽  
RC Aronoff
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Female Patient ◽  
Surgical Management ◽  
Ectodermal Dysplasia ◽  
Review Of The Literature ◽  
Rare Congenital Anomaly ◽  
Rare Syndrome ◽  
Clinical Triad ◽  
Musculoskeletal Involvement

Ectrodactyly-ectodermal dysplasia-clefting syndrome is a rare congenital anomaly that affects tissues of mesodermal and ectodermal origin. Musculoskeletal involvement frequently requires orthopedic intervention. The authors present a review of the literature pertaining to this rare syndrome as well as a case report of a female patient who exhibited the complete clinical triad. A description of the surgical management of her condition is also presented.

scholarly journals A rare case of eight multiple primary malignant neoplasms in a female patient: A case report and review of the literature

2014 ◽  
Vol 9 (2) ◽  
pp. 587-590 ◽  
Author(s):  
JIEMIN ZHAO ◽  
YAN TAN ◽  
YUGANG WU ◽  
WEI ZHAO ◽  
JUN WU ◽  
...  
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Rare Case ◽  
Malignant Neoplasms ◽  
Review Of The Literature ◽  
Multiple Primary

Gallbladder Paraganglioma: A Case Report With Review of the Literature

2005 ◽  
Vol 129 (4) ◽  
pp. 523-526 ◽  
Author(s):  
Shveta Mehra ◽  
Moonja Chung-Park
Keyword(s):  
Case Report ◽  
Retrospective Study ◽  
Family History ◽  
Gastrointestinal Bleeding ◽  
Biliary System ◽  
Rare Tumor ◽  
Review Of The Literature ◽  
Quadrant Pain ◽  
Endocrine Neoplasia ◽  
History Of

Abstract We report a case of gallbladder paraganglioma that was discovered during nonrelated surgery. Retrospective study disclosed a family history of pheochromocytoma. The occurrence of gallbladder paraganglioma in the presence of family history of endocrine neoplasia supports that gallbladder paraganglioma may indeed occur as a part of the multiple endocrine neoplasm syndrome. Gallbladder paraganglioma is a rare tumor, and so far to our knowledge only 6 cases have been reported in the literature. Three cases were discovered incidentally during cholecystectomy for cholelithiasis, 2 presented with right upper quadrant pain, and 1 manifested with gastrointestinal bleeding. We herein review all reported cases of paraganglioma of gallbladder and biliary system.

Mucocele of appendix: a case report

2021 ◽  
pp. 1-7
Author(s):  
Fareeha Farooqui ◽  
Sehrish Latif ◽  
Humera Naz Altaf ◽  
Sania Waseem ◽  
Sohaib Khan ◽  
...  
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Gastrointestinal Tract ◽  
Surgical Management ◽  
Iliac Fossa ◽  
Mucinous Cystadenoma ◽  
Right Hemicolectomy ◽  
Unusual Presentation ◽  
Rare Tumor ◽  
Malignant Changes

Abstract Mucinous cystadenoma is a rare tumor of appendix it accounts for only 0.4% of the gastrointestinal tract malignancies and is reported rarely in literature. Therefore the surgical management is not yet established. Here we report a case of a 65 year old female who presented with a dragging sensation and a feeling of mass in right iliac fossa. Her computed tomography (CT) suggested an abscess formation of the parietal peritoneum. She was planned for laparotomy and upon exploration a mass was found arising from tip of retroperitoneal appendix. Whole of the appendix was studded with mucoid material. Limited right hemicolectomy was performed and histopathology of appendix showed mucinous cystadenoma with no evidence of malignant changes. Patient remained uneventful and was discharged on 4th post operative day. The unusual presentation of retroperitoneal pseudomyxoma without any intraperitoneal pathology, prompted us to report this case. Continuous...

True Giant Ruptured Superficial Femoral Artery Aneurysm in Nonagenarian Female Patient: A Case Report and Review of the Literature

2019 ◽  
Vol 56 ◽  
pp. 353.e13-353.e17 ◽  
Author(s):  
Edoardo Frola ◽  
Emanuele Ferrero ◽  
Pia Cumbo ◽  
Fabiana Zandrino ◽  
Andrea Gaggiano
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Femoral Artery ◽  
Superficial Femoral Artery ◽  
Artery Aneurysm ◽  
Review Of The Literature

MEDICAL AND SURGICAL MANAGEMENT OF PARANEOPLASTIC PYODERMA GANGRENOSUM - A CASE REPORT AND REVIEW OF THE LITERATURE

2010 ◽  
Vol 65 (1) ◽  
pp. 37-40 ◽  
Author(s):  
S. Lamet ◽  
A. Bracke ◽  
E. Geluykens ◽  
E. Vlieghe ◽  
K. Seymons ◽  
...  
Keyword(s):  
Case Report ◽  
Surgical Management ◽  
Pyoderma Gangrenosum ◽  
Review Of The Literature

scholarly journals Monophasic Synovial Sarcoma of the Infratemporal Fossa—Case Report and Review of the Literature

2017 ◽  
Vol 13 (01) ◽  
pp. 01
Author(s):  
Ignacio Mendoza ◽  
Ilson Sepúlveda ◽  
Geraldine Ayres ◽  
◽  
◽  
...  
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
South America ◽  
Head And Neck ◽  
Synovial Sarcoma ◽  
Infratemporal Fossa ◽  
Soft Tissue Sarcomas ◽  
Complete Resection ◽  
Review Of The Literature ◽  
Histological Features

Synovial sarcoma (SS) represents about 10% of all soft tissue sarcomas. It is believed that its origin would be found in cells that are related neither to ultrastructural nor to histological features of the synovial tissue. Head and neck is very rarely affected, with the lower extremities being most frequent. Complete resection with or without radiotherapy and chemotherapy is currently considered the best available therapy. This time we present the case of a patient with SS located in the infratemporal fossa, its diagnosis, treatment and evolution. According to our knowledge it is the first reported case in South America.

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