scholarly journals Posttraumatic Rupture of Branch Pseudoaneurysm of Deep Femoral artery: A Rare Case

2019 ◽  
Vol 5 (02) ◽  
pp. 58-61
Author(s):  
Rajendra Prasad ◽  
Luv Luthra ◽  
Adharsh Maruthu
Keyword(s):  
Case Report ◽  
Femoral Artery ◽  
Rare Case ◽  
Sports Injuries ◽  
Severe Anemia ◽  
Rare Entity ◽  
Deep Femoral Artery ◽  
Femur Fractures ◽  
Pulsatile Mass ◽  
Thigh Swelling

Abstract Introduction Traumatic pseudoaneurysms of deep femoral artery (DFA) are usually seen secondary to sports injuries, postendovascular procedures, trauma to thigh, or after orthopaedic interventions for femur fractures. They usually present as either a pulsatile mass or even as thigh compartment syndrome if not diagnosed early. Case Report We present a case of a 65-year-old male who was referred for thigh swelling with severe anemia. On angiographic evaluation, patient was diagnosed to have pseudoaneurysm of DFA branch with hematoma in the thigh. Patient underwent an emergency surgery in view of hemodyanamic instability and ligation of ruptured DFA branch pseudoaneurysm. Conclusion Pseudoaneurysms of the DFA are rare entity and can be asymptomatic or may present with active bleeding in the compartment on rupture. Both surgical and endovascular treatments are available options and mainly depend on the hemodyanamic condition of the patient.

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.

scholarly journals Case Report: A giant myopericytoma involving the occipital region of the scalp - a rare entity

F1000Research ◽  
2016 ◽  
Vol 5 ◽  
pp. 2905 ◽  
Author(s):  
Sunil Munakomi ◽  
Pramod Chaudhary
Keyword(s):  
Smooth Muscle ◽  
Case Report ◽  
Histological Examination ◽  
Rare Case ◽  
Smooth Muscle Actin ◽  
Positive Staining ◽  
Occipital Region ◽  
Rare Entity ◽  
Muscle Actin ◽  
Complete Excision

Herein we report a rare case of a giant myopericytoma presenting in a 16-year-old girl as a slowly progressive swelling involving the scalp in the occipital region. It was managed by complete excision. Histological examination of the lesion revealed  spindle-shaped cells forming characteristic rosettes around the blood vessels, and positive staining with smooth muscle actin.

scholarly journals A rare case of multiple aneurysms in ilio-femoro-popliteal segment with rupture of deep femoral artery

Cor et Vasa ◽  
2017 ◽  
Vol 59 (5) ◽  
pp. e488-e492
Author(s):  
L. Beshev ◽  
T. Andreev ◽  
A. Marinov ◽  
N. Totsev ◽  
V. Velikov ◽  
...  
Keyword(s):  
Femoral Artery ◽  
Rare Case ◽  
Deep Femoral Artery ◽  
Multiple Aneurysms

scholarly journals Intersphincteric epidermoid inclusion cyst: report of a rare case

2020 ◽  
Vol 2020 (3) ◽  
Author(s):  
James Ashcroft ◽  
Betania Mahler-Araujo ◽  
Richard J Davies
Keyword(s):  
Case Report ◽  
Surgical Technique ◽  
Rare Case ◽  
Unusual Case ◽  
Accurate Diagnosis ◽  
Rare Entity ◽  
Inclusion Cyst ◽  
Patient Morbidity ◽  
Perineal Region ◽  
Epidermoid Inclusion Cyst

Abstract Epidermoid inclusion cysts of the perineal region are a rare entity, which require appropriate diagnosis and management. Here we describe the unusual case of a large protruding epidermoid inclusion cyst originating from the intersphincteric anal plane, which was mobilized and excised successfully. Essential investigations to ensure accurate diagnosis in addition to surgical technique to reduce recurrence and patient morbidity are described in this case report.

Congenital cholesteatoma in identical twins

2012 ◽  
Vol 127 (1) ◽  
pp. 67-69 ◽  
Author(s):  
T Al Balushi ◽  
J Z Naik ◽  
M Al Khabori
Keyword(s):  
Case Report ◽  
World Literature ◽  
Rare Case ◽  
Identical Twins ◽  
Rare Entity ◽  
Ear Surgery ◽  
Congenital Cholesteatoma ◽  
The World ◽  
Local Trauma ◽  
Clinical Pictures

AbstractObjective:We present an extremely rare case of congenital cholesteatoma in identical twins.Method:Case report of congenital cholesteatoma in identical twins, and a literature review, are presented.Results:Both cases presented to the ENT out-patient clinic, but with different clinical pictures. Both were managed surgically.Conclusion:Congenital cholesteatoma presents as a whitish mass in the middle ear, with an intact tympanic membrane. It is a rare entity comprising between 3.7 and 24 per cent of total cholesteatoma cases. The key to its diagnosis is the absence of previous ear infection, ear surgery and local trauma. To our best knowledge, this paper represents the first report in the world literature of congenital cholesteatoma in identical twins.

Intraoral Schwannoma: A Rare Case Report

2016 ◽  
Vol 1 (1) ◽  
pp. 20-22
Author(s):  
Ranjan Agrawal ◽  
Prashant Bhardwaj ◽  
Abhinav Srivastava
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Rare Case ◽  
Rare Entity ◽  
Rare Occurrence ◽  
Floor Of The Mouth ◽  
Nerve Sheath ◽  
Rare Case Report ◽  
Sheath Cells

ABSTRACT Schwannomas or neurilemmomas are benign, encapsulated tumor arising from nerve sheath cells. Intracranial Schwannomas are most common with rare occurrence in the extracranial region. It rarely occurs in the floor of the mouth with very few cases reported. We present a rare case report of Schwannoma of the floor of the mouth, thereby highlighting the consideration of this rare entity as one of the differential diagnosis in cases who present to us with swelling of the floor of the mouth and also the importance of immunohistochemistry in coming to the diagnosis. How to cite this article Srivastava A, Mohan C, Bhardwaj P, Agrawal R. Intraoral Schwannoma: A Rare Case Report. Int J Adv Integ Med Sci 2016;1(1):20-22.

scholarly journals Pyogenic infection of the hip joint as a complication of a femoral artery vascular access for percutaneous coronary intervention

2018 ◽  
Vol 12 (5) ◽  
pp. 155-160
Author(s):  
Jaroslaw Ucieklak ◽  
Robert Michał Proczka
Keyword(s):  
Percutaneous Coronary Intervention ◽  
Case Report ◽  
Vascular Access ◽  
Hip Joint ◽  
Femoral Artery ◽  
Stent Implantation ◽  
Rare Case ◽  
Coronary Intervention ◽  
Pyogenic Infection ◽  
Percutaneous Coronary

A rare case of clinical complication following a percutaneous coronary intervention is presented. A femoral vascular access was chosen to treat a coronary lesion with a stent implantation. This femoral vascular access, however, resulted in a pyogenic infection of the ipsilateral hip joint that was not properly diagnosed for an extended post-interventional period. The hip joint completely deteriorated before its underlying cause was identified. This case report illustrates the importance of recognizing potential endovascular complications independently of their frequency.

scholarly journals Dysembryoplastic neuropithelial tumor: a rare case report

2017 ◽  
Vol 5 (5) ◽  
pp. 2270
Author(s):  
Shailesh Thanvi ◽  
Hemant Jangid ◽  
Yogi Raj Joshi
Keyword(s):  
Young Adults ◽  
Case Report ◽  
Rare Case ◽  
Male Child ◽  
Adjuvant Chemoradiotherapy ◽  
Rare Entity ◽  
Intractable Seizures ◽  
Rare Case Report ◽  
Children And Young Adults ◽  
Space Occupying Lesion

Dysembryoplastic neuropithelial tumor (DNET) is a rare recently described, benign glioneural tumor frequently associated with intractable seizures in children and young adults which is important to recognise clinically and radiologically as it is surgically curable without need for adjuvant chemoradiotherapy. We hereby present a case report of a 10year old male child who presented with intractable seizures and right parietal space occupying lesion which was diagnosed DNET radiologically, treated by microsurgical excision and confirmed histopathologically as DNET, thus emphasising multidisciplinary role in management of this rare entity.

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