Charcot Joint
نویسندگان
چکیده
منابع مشابه
Reconstruction of Lisfranc joint dislocations secondary to Charcot neuroarthropathy using a plantar plate.
Lisfranc joint dislocation secondary to Charcot arthropathy is a debilitating condition that often leads to ulceration and infection. After conservative treatment, such as bracing and appropriate shoe wear fail, the only option might be amputation. However, we have seen good clinical outcomes from applying a plate to the plantar (tension) side of the medial midfoot. In our retrospective study, ...
متن کاملCharcot Elbow Joint as the Initial Symptom in Chiari Malformation with Syringomyelia.
Charcot joint (CJ), also known as neurotrophic arthropathy, is secondary to diabetes, syringomyelia, spinal tuberculosis, etc. The clinical manifestations are varied. The main performance includes pain, slightly restricted joint movement and very obvious swelling and damage of joint. It is easy to be misdiagnosed when the joint is the first symptom. We report a case of Charcot elbow joint as th...
متن کاملCharcot Joint of the Spine with Long Term Survival and Return to Near Full Function
Charcot joints of the spine are rare entities which mimic low grade soft tissue malignancies by appearing as a destructive mass lesion on radiographic studies. We report a 42-year-old diabetic female, who presented with a mass-like lesion of the thoracic spine extending into the posterior mediastinum. She presented with hemiplegia. With conservative treatment and without mechanical stabilizatio...
متن کاملCharcot-Leyden Crystals in Hodgkin's Lym-phoma
Herein, we reported on a middle-aged woman presented with painless cervical lymphadenopathy. Past medical history was not significant. Pathologic examination of incisional biopsy show partial effacement of lymph node architecture with many reactive inflammatory cells admixed with Reed-Sternberg cells, many Charcot-Leyden crystals, and noncaseating granuloma. Immunohistochemical staining was pos...
متن کاملCharcot-Marie-Tooth disease
Charcot-Marie-Tooth (CMT) disease is the most prevalent peripheral inherited neuropathy (1/2500 to 10 000; 2.8/10 000 in Spain), and the mean age at onset is 16 years (range 2 to 50 years, but presentation in the early infancy and as late as the 80's has been reported). Patients present with motor and sensory polyneuropathic semiology (distal lower limb weakness and atrophy, gait abnormalities ...
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ژورنال
عنوان ژورنال: Journal of UOEH
سال: 1982
ISSN: 0387-821X,2187-2864
DOI: 10.7888/juoeh.4.185