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[biomedres]

Chondroblastoma of the Medial Malleolus: A Very Rare Case with Radiopathological Correlation

Chondroblastoma of the Medial Malleolus: A Very Rare Case with Radiopathological Correlation in Biomedical Journal of Scientific & Technical Research

https://biomedres.us/fulltexts/BJSTR.MS.ID.006057.php

Chondroblastoma is an uncommon osseous neoplasm. It accounts for less than 1% of all bone tumors. Tumors of the medial malleolus are rare, and even rarer is the chondrogenic tumors of the medial malleolus [1]. The most common anatomical site involved by this tumor is the proximal humerus, followed by the distal femur, proximal femur, proximal tibia, talus and innominate bone, in descending order. The typical radiological finding is an eccentric osteolytic lesion, frequently accompanied by a thin sclerotic rim [2,3]. The male to female ratio is greater than 2:1, with peak incidence at age of 16 years. The proximal tibia is the most common location; but there is near even distribution of cases between the proximal tibia, proximal humerus, proximal femur, and distal femur [4-6]. Malignant transformation in chondroblastoma has been described in only a few cases [7]. Patients usually present with pain and swelling, particularly if a pathological fracture is present [8]. Chondroblastoma is usually treated by simple curettage with bone grafting [4,9].

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Company's Court Winding Up List 24.06.2020

Company’s Court Winding Up List 24.06.2020

ROLLS BUILDING

REMOTE HEARINGS IN HEARING ROOM 7

Before CHIEF INSOLVENCY AND COMPANIES JUDGE BRIGGS

Wednesday 24 June 2020 At 10:30 AM

Winding Up Petitions By Skype

HMRC Cases

CR-2018-006057 RICHARD MICHAEL GANDY & BERLIANA GANDY T/A LONDON WATERLOO HOSTEL

CR-2019-004958 MANOR ELECTRONICS LTD

CR-2019-005464 ST ANTHONY’S BREAD LIMITED

CR-2019-006299 B.E. DRYLINING LIMITED

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[biomedres]

Chondroblastoma of the Medial Malleolus: A Very Rare Case with Radiopathological Correlation

Chondroblastoma of the Medial Malleolus: A Very Rare Case with Radiopathological Correlation Biomedical Journal of Scientific & Technical Research

https://biomedres.us/fulltexts/BJSTR.MS.ID.006057.php

Tumors of the medial malleolus are a rare entity, with chondrogenic tumors of the medial malleolus being extremely rare. Very few cases of chondroblastoma of the medial malleolus are reported in the literature at present. We report a case of 29 years old male with swelling over the left medial malleolus. Radiological features favored the diagnosis of chondroblastoma, which was further confirmed by histopathological examination. The appearance of chondroblastoma at a very uncommon site has been discussed with its clinical and radiographic features, differential diagnosis and management. This case appears to be one of the very few reported cases of chondroblastoma occurring at medial malleolus. The present case report will increase the awareness of this rare tumor occurring at this unusual site, thereby avoiding any chance of misdiagnosis.

Learning Objectives

a) To describe the radiologic spectrum of chondroblastoma in a very uncommon site like medial malleolus, its differentials, and complications. b) To define the diagnosis of chondroblastoma in an appropriate clinical setting. c) To analyze the radiographic and MRI findings of chondroblastoma, to improve the diagnosis of this kind of tumor.

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bjstr

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[biomedres]

Chondroblastoma of the Medial Malleolus: A Very Rare Case with Radiopathological Correlation - BJSTR Journals

Chondroblastoma of the Medial Malleolus: A Very Rare Case with Radiopathological Correlation by Biomedical Journal of Scientific & Technical Research

https://biomedres.us/fulltexts/BJSTR.MS.ID.006057.php

Tumors of the medial malleolus are a rare entity, with chondrogenic tumors of the medial malleolus being extremely rare. Very few cases of chondroblastoma of the medial malleolus are reported in the literature at present. We report a case of 29 years old male with swelling over the left medial malleolus. Radiological features favored the diagnosis of chondroblastoma, which was further confirmed by histopathological examination. The appearance of chondroblastoma at a very uncommon site has been discussed with its clinical and radiographic features, differential diagnosis and management. This case appears to be one of the very few reported cases of chondroblastoma occurring at medial malleolus. The present case report will increase the awareness of this rare tumor occurring at this unusual site, thereby avoiding any chance of misdiagnosis.

Learning Objectives

a) To describe the radiologic spectrum of chondroblastoma in a very uncommon site like medial malleolus, its differentials, and complications. b) To define the diagnosis of chondroblastoma in an appropriate clinical setting. c) To analyze the radiographic and MRI findings of chondroblastoma, to improve the diagnosis of this kind of tumor.

For more articles on Journals on Biomedical Sciences click here

bjstr

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Companies Court Winding Up List 08.10.19

Companies Court Winding Up List 08.10.19

Rolls Buildings Court 1 Before INSOLVENCY AND COMPANIES COURT JUDGE BARBER

Wednesday 9 October 2019 Robed At 10:30 AM

CR-2018-006057 RICHARD MICHAEL GANDY & BERLIANA GANDY T/A LONDON WATERLOO HOSTEL

CR-2018-007083 Clarendon House Watford Ltd

CR-2019-000831 ROCHESTER INVESTMENT PARTNERS

CR-2019-002272 MAYBROSE LIMITED

CR-2019-002901 DOORDECK LIMITED

CR-2019-002951 COURTVIEW…