Traumatic Fracture in a patient of Osteopoikilosis with review of literature

Introduction: Osteopoikilosis or osteopathia condensans disseminata is a rare hereditary autosomal dominant sclerosing bone dysplasia. Patients are usually asymptomatic and the diagnosis is usually made incidentally on radiographs which show presence of symmetric, multiple, well defined, small ovoi...

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Main Authors: Rohan Bansal, Aditya C Pathak, Binoti Sheth, Atul K Patil
Format: Article
Language:English
Published: Indian Orthopaedic Research Group 2013-04-01
Series:Journal of Orthopaedic Case Reports
Online Access:http://www.jocr.co.in/wp/2013/04/13/2250-0685-095-fulltext/
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spelling doaj-b9a6dd72018a42ad8e34b1a5c358a7052020-11-24T22:19:19ZengIndian Orthopaedic Research GroupJournal of Orthopaedic Case Reports2250-06852013-04-0132162010.13107/jocr.2250-0685.095Traumatic Fracture in a patient of Osteopoikilosis with review of literatureRohan Bansal0Aditya C Pathak1Binoti Sheth2Atul K Patil3Department Of Orthopaedics, Government Medical College, Miraj and PVPGH, Sangli. IndiaDr LH Hiranandani Hospital, Powaii, MumbaiDepartment of Orthopaedics, Lokmanya Tilak Medical College & Sion Hospital, Mumbai. IndiaDepartment of Orthopaedics, Lokmanya Tilak Medical College & Sion Hospital, Mumbai. IndiaIntroduction: Osteopoikilosis or osteopathia condensans disseminata is a rare hereditary autosomal dominant sclerosing bone dysplasia. Patients are usually asymptomatic and the diagnosis is usually made incidentally on radiographs which show presence of symmetric, multiple, well defined, small ovoid areas of increased radiodensity clustered in peri-articular osseous regions with propensity for epiphyseal and metaphyseal involvement. There are no increased risks of pathological fracture in a case of osteopoikilosis and traumatic fracture healing in a case of osteopoikilosis is similar to fracture occurring in other normal patients. Case Report: A 34 years male, electrician came with history of accidental fall from height while working in office leading to development of pain and swelling over left lower leg and ankle diagnosed with Ruedi-Allgower classification type I pilon fracture(without fibula fracture) no distal neuro-vascular deficit. Patient was offered surgical treatment in form of open reduction and internal fixation of tibial fracture by plate osteosynthesis using antero-medial approach , showed complete union and was followed up for eight months. Conclusion: Osteopoikilosis has a benign course and it should always be kept as a possible differential diagnosis for osteoblastic metastasis to avoid diagnositic dilemma. Diagnosis can be settled by routine x-rays ( for type ,extent and site of lesions, bones affected), clinical features of patient , histopathology and other systemic or pre-existing conditions. Keywords: Fracture , Osteopoikilosis , union, Pilon, Osteoblastic metastasishttp://www.jocr.co.in/wp/2013/04/13/2250-0685-095-fulltext/
collection DOAJ
language English
format Article
sources DOAJ
author Rohan Bansal
Aditya C Pathak
Binoti Sheth
Atul K Patil
spellingShingle Rohan Bansal
Aditya C Pathak
Binoti Sheth
Atul K Patil
Traumatic Fracture in a patient of Osteopoikilosis with review of literature
Journal of Orthopaedic Case Reports
author_facet Rohan Bansal
Aditya C Pathak
Binoti Sheth
Atul K Patil
author_sort Rohan Bansal
title Traumatic Fracture in a patient of Osteopoikilosis with review of literature
title_short Traumatic Fracture in a patient of Osteopoikilosis with review of literature
title_full Traumatic Fracture in a patient of Osteopoikilosis with review of literature
title_fullStr Traumatic Fracture in a patient of Osteopoikilosis with review of literature
title_full_unstemmed Traumatic Fracture in a patient of Osteopoikilosis with review of literature
title_sort traumatic fracture in a patient of osteopoikilosis with review of literature
publisher Indian Orthopaedic Research Group
series Journal of Orthopaedic Case Reports
issn 2250-0685
publishDate 2013-04-01
description Introduction: Osteopoikilosis or osteopathia condensans disseminata is a rare hereditary autosomal dominant sclerosing bone dysplasia. Patients are usually asymptomatic and the diagnosis is usually made incidentally on radiographs which show presence of symmetric, multiple, well defined, small ovoid areas of increased radiodensity clustered in peri-articular osseous regions with propensity for epiphyseal and metaphyseal involvement. There are no increased risks of pathological fracture in a case of osteopoikilosis and traumatic fracture healing in a case of osteopoikilosis is similar to fracture occurring in other normal patients. Case Report: A 34 years male, electrician came with history of accidental fall from height while working in office leading to development of pain and swelling over left lower leg and ankle diagnosed with Ruedi-Allgower classification type I pilon fracture(without fibula fracture) no distal neuro-vascular deficit. Patient was offered surgical treatment in form of open reduction and internal fixation of tibial fracture by plate osteosynthesis using antero-medial approach , showed complete union and was followed up for eight months. Conclusion: Osteopoikilosis has a benign course and it should always be kept as a possible differential diagnosis for osteoblastic metastasis to avoid diagnositic dilemma. Diagnosis can be settled by routine x-rays ( for type ,extent and site of lesions, bones affected), clinical features of patient , histopathology and other systemic or pre-existing conditions. Keywords: Fracture , Osteopoikilosis , union, Pilon, Osteoblastic metastasis
url http://www.jocr.co.in/wp/2013/04/13/2250-0685-095-fulltext/
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