scholarly journals Odontogenic Myxoma of the Anterior Mandible: Case Report of a Rare Entity and Review of the Literature

2021 ◽  
Author(s):  
Maryam Sohrabi ◽  
Ramtin Dastgir
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Treatment Plan ◽  
Chief Complaint ◽  
Anterior Region ◽  
Rare Entity ◽  
Review Of The Literature ◽  
Odontogenic Myxoma ◽  
Anterior Mandible

We report a case of a 38-year-old female patient with odontogenic myxoma who was referred to us with chief complaint of a persistent painful lesion and teeth mobility in the anterior region of the mandible which had underwent a faulty treatment plan in an outside clinic.

scholarly journals Congenital Trans Mesenteric Hernia (CTMH) in a Female Patient with Familial Mediterranean fever (FMF): Case Report and Review of the Literature

2019 ◽  
Vol 4 (1) ◽  
Keyword(s):  
Abdominal Pain ◽  
Case Report ◽  
Female Patient ◽  
Surgical Repair ◽  
Exploratory Laparotomy ◽  
Rare Entity ◽  
Review Of The Literature ◽  
Hernia Defect ◽  
Mediterranean Fever ◽  
Mesenteric Hernia

Congenital Trans mesenteric Hernia (CTMH) is a rare entity of internal hernia that occur as a congenital defect in children due to an error in the rotation of the midget, presenting usually with an abdominal pain, fever and bilious vomiting. However, if left untreated, disastrous outcomes such as acute bowel obstruction and strangulation can take place. Its diagnosis is sometimes challenging to physicians and requires exploratory laparotomy to confirm the presence of a hernia defect. CT scan prior to surgery is seldom needed and may not have a benefit to guide for the exact diagnosis. For treatment, surgical repair, either open or laparoscopic, is the procedure of choice to manage such a condition. We report a case of CTMH in a 3.5–year-old female patient who presented to our hospital with abdominal pain and inconsolable crying.

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

BOWENOID BASAL CELL CARCINOMA OF THE THUMB: A CASE REPORT AND REVIEW OF THE LITERATURE

Hand Surgery ◽  
2002 ◽  
Vol 07 (02) ◽  
pp. 295-298 ◽  
Author(s):  
M. Galeano ◽  
M. Colonna ◽  
M. Lentini ◽  
F. Stagno D'Alcontres
Keyword(s):  
Case Report ◽  
Basal Cell Carcinoma ◽  
Cell Carcinoma ◽  
Basal Cell ◽  
Basal Layer ◽  
Rare Entity ◽  
Review Of The Literature ◽  
Skin Malignancy ◽  
Root Sheath ◽  
Common Skin

Basal cell carcinoma (BCC) is the most common skin malignancy arising from cells of the basal layer of the epithelium or from the external root sheath of the hair follicle. BCC of the digit is a rare entity. The article presents one such case of bowenoid BCC of the thumb which required amputation at the MP joint.

scholarly journals Dysgenetic Polycystic Disease of Minor Salivary Gland: A Rare Case Report and Review of the Literature

2017 ◽  
Vol 2017 ◽  
pp. 1-5
Author(s):  
N. Srikant ◽  
Shweta Yellapurkar ◽  
Karen Boaz ◽  
Mohan Baliga ◽  
Nidhi Manaktala ◽  
...  
Keyword(s):  
Differential Diagnosis ◽  
Salivary Gland ◽  
Case Report ◽  
Rare Case ◽  
Minor Salivary Gland ◽  
Rare Entity ◽  
Review Of The Literature ◽  
Lower Lip ◽  
Polycystic Disease ◽  
Rare Case Report

Polycystic (dysgenetic) disease of the salivary glands is a rare entity that has only recently been described in the literature. The disease is more commonly seen in females and majority of the cases have presented as bilateral parotid gland swellings. This case presenting in a 21-year-old male is the first of this unusual entity involving solely the minor salivary gland on the lower lip. This case report highlights the importance for the clinician to be aware of this differential diagnosis, when treating an innocuous lesion like a mucocele.

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

scholarly journals Olfactory Nerve Schwannoma: A Case Report and Review of the Literature

2018 ◽  
Vol 04 (03) ◽  
pp. e164-e166 ◽  
Author(s):  
Mahmoud Taha ◽  
Amr AlBakry ◽  
Magdy ElSheikh ◽  
Tarek AbdelBary
Keyword(s):  
Case Report ◽  
Peripheral Nerves ◽  
Traffic Accident ◽  
Road Traffic ◽  
Olfactory Nerve ◽  
Anterior Cranial Fossa ◽  
Benign Tumors ◽  
Rare Entity ◽  
Review Of The Literature ◽  
Cranial Fossa

AbstractSchwannomas are benign tumors, which arise from the Schwann cells of the central or peripheral nerves. They form 8% of all intracranial tumors and most of the cases arise from vestibular division of the 8th cranial nerve. Rare cases are shown to arise from the olfactory or optic nerve, being devoid of myelin sheath. Up to date and according to our best of knowledge, 66 cases have been reported till now. Here we present a review of the literature and a case report of a 56-year-old male with an accidently discovered anterior cranial fossa schwannoma, following a road traffic accident. Tumor was completely excised, using a right frontal approach. Histopathology revealed Antoni-A cellular pattern. Although rare, but olfactory nerve schwannomas should be included in the differential diagnosis in anterior cranial fossa space occupying lesions, and the approach should be designed taking into consideration, this rare entity.

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