Tang Hsi Ryu syndrome: Difference between revisions
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(Created page with "__NOTOC__ {{SI}} {{CMG}}; {{AE}} {{RT}} ==Overview== Tang Hsi Ryu syndrome is a very rare disease involving skin, liver, spleen and peripheral nerves. ==Pathoph...") |
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====Abdomen==== | ====Abdomen==== | ||
* [[Hepatosplenomegaly]] | * [[Hepatosplenomegaly]] | ||
* [[Ascites]] | * [[Ascites]]<ref name="pmid6663309">{{cite journal |author=Tang LM, Hsi MS, Ryu SJ, Minauchi Y |title=Syndrome of polyneuropathy, skin hyperpigmentation, oedema and hepatosplenomegaly |journal=J. Neurol. Neurosurg. Psychiatr. |volume=46 |issue=12 |pages=1108–14 |year=1983 |month=December |pmid=6663309 |pmc=491776 |doi= |url=}}</ref> | ||
====Extremities==== | ====Extremities==== |
Latest revision as of 16:17, 2 August 2012
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Raviteja Guddeti, M.B.B.S. [2]
Overview
Tang Hsi Ryu syndrome is a very rare disease involving skin, liver, spleen and peripheral nerves.
Pathophysiology
In Japan and United States this syndrome has been associated with plasma cell dyscrasia.
Diagnosis
Physical Examination
Skin
Head
Abdomen
Extremities
Neurologic
Others