An Adolescent with Progressive Enlargement of Digits: Case report and proposed diagnostic criteria for macrodystrophia lipomatosa
Macrodystrophia lipomatosa (ML) is a rare congenital non-hereditary condition caused by an increase in all mesenchymal elements. We report a 14-year-old girl who presented to the Medical Outpatient Department, Kunhitharuvai Memorial Charitable Trust Medical College, Kozhikode, India, in 2017 with pr...
Main Authors: | , |
---|---|
Format: | Article |
Language: | English |
Published: |
Sultan Qaboos University
2019-03-01
|
Series: | Sultan Qaboos University Medical Journal |
Online Access: | https://journals.squ.edu.om/index.php/squmj/article/view/3004 |
id |
doaj-93e24f70c14549fbae44b01471776d52 |
---|---|
record_format |
Article |
spelling |
doaj-93e24f70c14549fbae44b01471776d522020-11-25T02:43:11ZengSultan Qaboos UniversitySultan Qaboos University Medical Journal 2075-051X2075-05282019-03-0118455355610.18295/squmj.2018.18.04.0232543An Adolescent with Progressive Enlargement of Digits: Case report and proposed diagnostic criteria for macrodystrophia lipomatosaBinoy J. Paul0Raveendran A. V.1Department of Medicine & Rheumatology, Kunhitharuvai Memorial Charitable Trust Medical College, Kozhikode, IndiaDepartment of Internal Medicine, Government Medical College, Kozhikode, IndiaMacrodystrophia lipomatosa (ML) is a rare congenital non-hereditary condition caused by an increase in all mesenchymal elements. We report a 14-year-old girl who presented to the Medical Outpatient Department, Kunhitharuvai Memorial Charitable Trust Medical College, Kozhikode, India, in 2017 with progressive enlargement of digits. An X-ray and T1-weighted magnetic resonance imaging scan showed enlargement of the phalanges of the middle and index finger of the left hand with an overgrowth of soft tissues. The patient was subsequently diagnosed with ML. As the condition is benign and usually asymptomatic, no medical treatment was deemed necessary. This report describes a case of ML and proposes a set of diagnostic criteria to aid clinicians in the differential diagnosis of the condition. Keywords: Congenital Disorders; Gigantism; Macrodactyly of the Hand; Differential Diagnosis; Case Report; India.https://journals.squ.edu.om/index.php/squmj/article/view/3004 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Binoy J. Paul Raveendran A. V. |
spellingShingle |
Binoy J. Paul Raveendran A. V. An Adolescent with Progressive Enlargement of Digits: Case report and proposed diagnostic criteria for macrodystrophia lipomatosa Sultan Qaboos University Medical Journal |
author_facet |
Binoy J. Paul Raveendran A. V. |
author_sort |
Binoy J. Paul |
title |
An Adolescent with Progressive Enlargement of Digits: Case report and proposed diagnostic criteria for macrodystrophia lipomatosa |
title_short |
An Adolescent with Progressive Enlargement of Digits: Case report and proposed diagnostic criteria for macrodystrophia lipomatosa |
title_full |
An Adolescent with Progressive Enlargement of Digits: Case report and proposed diagnostic criteria for macrodystrophia lipomatosa |
title_fullStr |
An Adolescent with Progressive Enlargement of Digits: Case report and proposed diagnostic criteria for macrodystrophia lipomatosa |
title_full_unstemmed |
An Adolescent with Progressive Enlargement of Digits: Case report and proposed diagnostic criteria for macrodystrophia lipomatosa |
title_sort |
adolescent with progressive enlargement of digits: case report and proposed diagnostic criteria for macrodystrophia lipomatosa |
publisher |
Sultan Qaboos University |
series |
Sultan Qaboos University Medical Journal |
issn |
2075-051X 2075-0528 |
publishDate |
2019-03-01 |
description |
Macrodystrophia lipomatosa (ML) is a rare congenital non-hereditary condition caused by an increase in all mesenchymal elements. We report a 14-year-old girl who presented to the Medical Outpatient Department, Kunhitharuvai Memorial Charitable Trust Medical College, Kozhikode, India, in 2017 with progressive enlargement of digits. An X-ray and T1-weighted magnetic resonance imaging scan showed enlargement of the phalanges of the middle and index finger of the left hand with an overgrowth of soft tissues. The patient was subsequently diagnosed with ML. As the condition is benign and usually asymptomatic, no medical treatment was deemed necessary. This report describes a case of ML and proposes a set of diagnostic criteria to aid clinicians in the differential diagnosis of the condition.
Keywords: Congenital Disorders; Gigantism; Macrodactyly of the Hand; Differential Diagnosis; Case Report; India. |
url |
https://journals.squ.edu.om/index.php/squmj/article/view/3004 |
work_keys_str_mv |
AT binoyjpaul anadolescentwithprogressiveenlargementofdigitscasereportandproposeddiagnosticcriteriaformacrodystrophialipomatosa AT raveendranav anadolescentwithprogressiveenlargementofdigitscasereportandproposeddiagnosticcriteriaformacrodystrophialipomatosa AT binoyjpaul adolescentwithprogressiveenlargementofdigitscasereportandproposeddiagnosticcriteriaformacrodystrophialipomatosa AT raveendranav adolescentwithprogressiveenlargementofdigitscasereportandproposeddiagnosticcriteriaformacrodystrophialipomatosa |
_version_ |
1724770982261948416 |