Early-onset Childhood Sarcoidosis with Incidental Multiple Enchondromatosis
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چکیده
منابع مشابه
Early-onset Childhood Sarcoidosis with Incidental Multiple Enchondromatosis
The triad of rash, arthritis, and uveitis seems to be characteristic for early-onset childhood sarcoidosis. We describe an interesting case of early-onset childhood sarcoidosis coexisting enchondromatosis, which clinically masquerade as Langerhans cell histiocytosis. A 33 months old girl presented with skin rash, subcutaneous nodules with polyarthritis, and revealed the involvement of lymph nod...
متن کاملA case of early onset renal sarcoidosis complecated with multiple enchondromatosis
Methods A five month old boy suffered from skin rash on his whole body after vaccination of BCG. At three years old, he developed fever and painless soft mass on his right ankle. Enhanced abdominal CT scan showed multiple low density lesions in both kidneys. He was initially diagnosed as having acute focal bacterial nephritis. However, antibiotics were not effective and he was referred to our h...
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S U M M A R Y — A 2 y e a r o l d b o y w a s a d m i t t e d o w i n g t o a s u b a c u t e e p i s o d e o f a t a x i c g a i t a n d h e a r i n g d e f i c i t . C o m p u t e r i z e d t o m o g r a p h y ( C T ) w a s n o r m a l a n d c e r e b r o s p i n a l f l u i d ( C S F ) a n a l y s i s r e v e a l e d g a m m a g l o b u l . n s l e v e l o f 1 5 . 4 % ( n o r m a l 7 t o 1 4...
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In contrast to solitary enchondroma,patients with multiple enchondromatosis of bone (Ollier's disease) get affected in childhood by bone swelling and growth retardation. In adults, the main problem is the risk of malign transformation up to 40%.Pain, increasing local tumor and thinning of the corticalis are the typical clinical and radiological signs of transformation to a low grade chondrosarc...
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Familial Blau syndrome and sporadic early-onset sarcoidosis (EOS) are both systemic granulomatous diseases evoked by the spontaneous activation of mutated NOD2. In Japan, the R334W amino acid substitution is more frequently identified, whereas the R334Q mutation is rare and, in contrast to western countries where disease causing mutations are typically hereditary, most Japanese cases derive fro...
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ژورنال
عنوان ژورنال: Journal of Korean Medical Science
سال: 2012
ISSN: 1011-8934,1598-6357
DOI: 10.3346/jkms.2012.27.1.96