Capillary leak syndrome differential diagnosis: Difference between revisions
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==Differential diagnosis== | ==Differential diagnosis== | ||
Due to overlapping clinical and laboratory findings of capillary leak syndrome with other conditions, it is considered as the diagnosis of exclusion. The following are the differential diagnoses considered in patients with systemic capillary leak syndrome: | |||
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!Differential diagnoses of Systemic Capillary Leak Syndrome | |||
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# Polycythemia vera | |||
# Hereditary angioedema | |||
# Gleich syndrome | |||
# Adrenal insufficiency | |||
# Mast cell disease | |||
# Acute gastroenteritis | |||
# Carcinoid syndrome | |||
# Primary amyloidosis | |||
# Chronic heart failure | |||
# Sepsis | |||
# Toxic shock syndrome | |||
|} | |||
==References== | ==References== | ||
Revision as of 00:42, 7 August 2022
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-In-Chief: M. Hassan, M.B.B.S
Differential diagnosis
Due to overlapping clinical and laboratory findings of capillary leak syndrome with other conditions, it is considered as the diagnosis of exclusion. The following are the differential diagnoses considered in patients with systemic capillary leak syndrome:
| Differential diagnoses of Systemic Capillary Leak Syndrome |
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