scholarly journals Osteoid Osteoma of the Ankle Posing As a Distal Tibiofibular Syndesmosis: A Rare Case Report

2016 ◽  
Vol 06 (02) ◽  
pp. 082-084
Author(s):  
Anand Kumar S. ◽  
Arjun Ballal ◽  
Anoop Hegde ◽  
A. Ponnambalam
Keyword(s):  
Case Report ◽  
Osteoid Osteoma ◽  
Rare Case ◽  
Full Range ◽  
Lower Limbs ◽  
Excision Biopsy ◽  
Common Symptom ◽  
Ankle Motion ◽  
Rare Case Report ◽  
The Common

AbstractOsteoid osteoma is a benign tumor of the bones. The adolescent males are the most commonly involved population. Pain of the affected site forms the common symptom during clinical presentation. The lower limbs are the most commonly affected site.We present here a case report of a middle aged gentleman who presented to us with complaints of pain and mass over the non-dominant ankle for four years. Clinical examination revealed a bony hard swelling proximal to the lateral malleolus. The radiographs and CT scan reports were consistent with features suggestive of an exostosis bridging the distal tibio-fibular syndesmosis. Surgical exploration revealed a mass with definite borders bridging the distal tibio-fibular syndesmosis. Excision biopsy was performed and the histopathology of the specimen reported features consistent with that of an osteoid osteoma. The patient was started on physiotherapy of the ankle and he was noted to have full range of ankle motion at six months. As no such case has been reported in earlier in literature we present it as a rare case report.

scholarly journals Osteoid osteoma in the hamate: A rare case report

2019 ◽  
Vol 8 (3) ◽  
pp. 1
Author(s):  
Tugrul Yildirim ◽  
Mehmet Armangil ◽  
Kerem Basarir
Keyword(s):  
Case Report ◽  
Osteoid Osteoma ◽  
Rare Case ◽  
Rare Case Report

scholarly journals The common peroneal nerve schwannoma: A case rare case report with brief review of literature

2020 ◽  
Vol 6 (4) ◽  
pp. 330-332
Author(s):  
Abhijeet Bele ◽  
◽  
Piyush Kumar Panchariya ◽  
H Singh ◽  
D Singh
Keyword(s):  
Case Report ◽  
Peroneal Nerve ◽  
Rare Case ◽  
Common Peroneal Nerve ◽  
Review Of Literature ◽  
Rare Case Report ◽  
The Common

scholarly journals Ossifying Fibroma of Dorsal Spine in a Postpartum Female: A Rare Case Report

2019 ◽  
Vol 08 (02) ◽  
pp. 136-138
Author(s):  
Musali Siddartha Reddy ◽  
Gollapudi Prakash Rao ◽  
Mohammed Imran ◽  
Uday Goutam Nookathota
Keyword(s):  
Case Report ◽  
Postpartum Period ◽  
Rare Case ◽  
Lower Limbs ◽  
Dorsal Spine ◽  
Postpartum Woman ◽  
Ossifying Fibroma ◽  
Diagnostic Dilemma ◽  
Spinal Stabilization ◽  
Rare Case Report

AbstractA rare case of monostotic ossifying fibroma of the dorsal spine in a postpartum woman is being described. Ossifying fibromas of the spine are very rare tumors. They are components of benign fibro-osseous lesions. We report a case of an 18-year-old woman, who presented with complaints of weakness of both the lower limbs in the immediate postpartum period and was diagnosed with ossifying fibroma of the dorsal [D3] vertebral body. The tumor was excised followed by spinal stabilization. Histopathologic findings were consistent with ossifying fibroma. Postoperative period was uneventful. Monostotic variant of ossifying fibroma in the dorsal spine is an extremely rare tumor, and its presence in the postpartum period adds on to the diagnostic dilemma. Hence this case report can be kept in mind while evaluating a case presenting with complaints of weakness of both the lower limbs in the immediate postpartum period.

Painless osteoid osteoma of tibia in a fifteen-month-old child: a rare case report

2010 ◽  
Vol 20 (5) ◽  
pp. 393-396
Author(s):  
Ashok Kumar ◽  
Manish Kumar Varshney ◽  
Dharmesh Khatri ◽  
Shah Alam Khan ◽  
C. S. Yadav ◽  
...  
Keyword(s):  
Case Report ◽  
Osteoid Osteoma ◽  
Rare Case ◽  
Rare Case Report

scholarly journals MRSA as a causative factor for ecthyma gangrenosum: a rare case report

2019 ◽  
Vol 10 (4) ◽  
pp. 2745-2747
Author(s):  
Kiran Madhusudhan ◽  
Madhusudhan
Keyword(s):  
Staphylococcus Aureus ◽  
Pseudomonas Aeruginosa ◽  
Case Report ◽  
Rare Case ◽  
Methicillin Resistant Staphylococcus Aureus ◽  
Causative Factor ◽  
Lower Limbs ◽  
Skin Manifestation ◽  
Ecthyma Gangrenosum ◽  
Rare Case Report

Ecthyma gangrenosum is a skin manifestation of Pseudomonas aeruginosa in immunocompromised individuals. Here we report a case of a 64-year-old diabetic female with Ecthyma gangrenosum lesions on both lower limbs, admitted for surgical debridement. Pus culture taken during surgery showed growth of Methicillin-resistant Staphylococcus aureus. The patient was started on appropriate antibiotics with reasonable glycemic control using parenteral insulin. The patient responded well to the above treatment and was discharged.

scholarly journals Nevus sebaceous of Jadassohn of face with infundibular and keratinous cyst in an adolescent Arab male-a rare case report

2018 ◽  
Vol 6 (3) ◽  
pp. 1033
Author(s):  
Scott Arockia Singh M. ◽  
Paul Raphel ◽  
Sneha Devadas ◽  
Siny Vellukara Sasidharan
Keyword(s):  
Case Report ◽  
Skin Lesion ◽  
Rare Case ◽  
Medical Literature ◽  
Interesting Case ◽  
Malignant Change ◽  
Excision Biopsy ◽  
Rare Case Report ◽  
The Face ◽  
Nevus Sebaceous

Nevus Sebaceous of Jadassohn is rare hamartomatous skin lesion. We report an interesting case of an Adolescent Arab male 18yr old, who presented to us with a velvety plaque of 7cm length in his left preauricular area. Excision biopsy revealed Nevus sebaceous of Jadassohn with infundibular and keratinous cyst. The lesion is present since birth started as a tiny lesion and grown to the current size. No such large sized lesion on the face has ever been reported in the medical literature till date. We advise an early excision as they have strong potential for malignant change.

scholarly journals Urinary Bladder Leiomyoma: A Rare Case Report

1970 ◽  
Vol 2 (2) ◽  
pp. 70-71
Author(s):  
HU Bhuiyan
Keyword(s):  
Case Report ◽  
Urinary Bladder ◽  
Key Words ◽  
Female Patient ◽  
Rare Case ◽  
Excision Biopsy ◽  
Key Words Urinary Bladder ◽  
Rare Case Report ◽  
Bladder Leiomyoma

A rare case of urinary bladder leiomyoma in a female patient is presented here. A quarter of these cases are asymptomatic only to be diagnosed by ultrasonography. Symptomatic cases are also misleading as in this case. Laparotomy, removal of mass and ultimately histopathology proved the case to be that of a urinary bladder leiomyoma. Ibrahim Med. Coll. J. 2008; 2(2): 70-71 Key Words: Urinary bladder leiomyoma, laparotomy, excision biopsy doi: 10.3329/imcj.v2i2.2943

scholarly journals Rectal migration of Ventriculo-peritonial shunt: a rare case report

2018 ◽  
Vol 32 (2) ◽  
pp. 303-305
Author(s):  
Anand Sharma ◽  
Avdesh Shukla ◽  
S.N. Iyengar
Keyword(s):  
Case Report ◽  
Ventriculoperitoneal Shunt ◽  
Management Strategy ◽  
Rare Case ◽  
Rare Complication ◽  
Colonic Perforation ◽  
Review Of Literature ◽  
Vp Shunt ◽  
Rare Case Report ◽  
The Common

Abstract Colonic perforation following ventriculoperitoneal shunt is a rare complication. The common treatment is to remove the perforating catheter and replace with new one. In this case report we reported a rare case of colonic perforation following VP shunt and its anal migration. We have discussed its pathogenesis, management strategy and review of literature.

Sign in / Sign up

Export Citation Format

Share Document