نتایج جستجو برای: macrodystrophia lipomatosa (mdl)

تعداد نتایج: 1891  

2011
Elpis Mantadakis Savvas Deftereos Efthimios Sivridis Lambros Michailidis Athanassios Chatzimichael Panos Prassopoulos

Introduction: Macrodystrophia lipomatosa (MDL) is a non-hereditary congenital developmental anomaly characterized by localized gigantism due to overgrowth of all mesenchymal elements. Case Report: The authors describe a case of macrodystrophia lipomatosa (MDL) with involvement of the median nerve in a 10-year-old girl and review the pathologic, radiographic, ultrasonographic and MR imaging char...

2013
Jae Hyun Kwon So Young Lim Ha Seong Lim

remaining three ulnar digits appeared normal. Magnetic resonance imaging (MRI) revealed characteristics of macrodystrophia lipomatosa such as enlargement and marked proliferation of the adipose tissues of the left hand, especially the radial aspect. MRI also demonstrated excessive fibrofatty tissue around the affected digits. This tissue has the same signal characteristics as fat on MRI, that i...

Journal: :Jornal of the Foot & Ankle 2023

Macrodystrophia lipomatosa (MDL) is a rare congenital disorder characterized by localized gigantism of one or several digits. It mayinvolve the entire limb due to progressive overgrowth all mesenchymal elements with an excessive increase in fibro-adiposetissues. occurs most commonly lower limbs. comes clinical attention for cosmetic reasons, mechanical problems secondaryto degenerative joint di...

2010
Rizwan A Khan Shagufta Wahab Ibne Ahmad Rajendra S Chana

AIM Macrodystrophia lipomatosa is a rare cause of gigantism of limb which can be confused with other common causes like congenital lymphedema. It presents usually with loss of function and cosmetic problems. Four cases are described with emphasis on clinical presentation, differential diagnoses, imaging and treatment options. METHODS & RESULTS Four patients of macrodystrophia lipomatosa were ...

2017
Rajesh Sharma Puneet Gupta Manik Mahajan Manjit Arora Anchal Gupta

Macrodystrophia lipomatosa is a rare entity that is mostly diagnosed in children. It has been very rarely reported in adults. Here, we describe the X-ray and computed tomography findings in a case of macrodystrophia lipomatosa in an elderly female presenting with an enlarged second toe since birth and bony outgrowths causing pressure effects and cosmetic problems.

Journal: :Journal of the Korean Radiological Society 1989

Journal: :medical journal of islamic republic of iran 0
maryam rahmani from the department of radiology, emam khomeini medical center; tehran university of medical sciences, tehran, i.r. iran. mohammad ali shabani

macrodystrophia lipomatosa is a rare congenital form of localized gigantism characterized by an increase in all mesenchymal elements, particularly fibroadipose tissue. mr imaging can be used to examine the soft tissue and detect the fibrous and fatty hypertrophy that characterizes this condition and also diagnose an associated fibrolipomatous hamartoma of the median or plantar nerve. we describ...

Journal: :Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie 2017
Romulus Fabian Tatu Dan Nelu Anuşca Alis Liliana Carmen Dema Lucian Petru Jiga Mihai Hurmuz Carmen Sofica Tatu Mihai Ionac Monica Adriana Vaida

Macrodystrophia lipomatosa is a rare, congenital, non-hereditary disease, characterized by local gigantism of the fingers or toes. We report the case of a 37-month-old boy, with no prior past medical history, who presented with a gigantic dystrophy of the left forefoot. The location of the deformity was involving the plantar and dorsal aspect of the foot, and digits 1 to 4. After clinical exami...

2015
Theddeus OH Prasetyono Enjeline Hanafi Windi Astriana

Macrodystrophia lipomatosa (MDL) is a rare congenital non-hereditary disorder that has significant impact on patient morbidity. This study provides a comprehensive review of the natural history, diagnosis, management, and outcomes of the disorder. A literature search in PubMed was conducted to identify cases of MDL from January 1950 to 14 February 2014. After ruling out articles without informa...

Journal: :Journal of Clinical Imaging Science 2011

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