Blue rubber bleb nevus syndrome differential diagnosis: Difference between revisions
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** Zones of lucency | ** Zones of lucency | ||
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|Familial Glomangiomatosis | |Familial Glomangiomatosis<ref name="pmid9577316">{{cite journal |vauthors=Iqbal A, Cormack GC, Scerri G |title=Hereditary multiple glomangiomas |journal=Br J Plast Surg |volume=51 |issue=1 |pages=32–7 |date=January 1998 |pmid=9577316 |doi= |url=}}</ref> | ||
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* Painful [[cutaneous]] lesions | |||
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|biopsy | |||
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|Genetics of Klippel-Trenaunay-Weber Syndrome | |Genetics of Klippel-Trenaunay-Weber Syndrome |
Revision as of 17:50, 6 December 2018
Overview
Blue rubber bleb nevus syndrome must be differentiated from dermatologic manifestations of kaposi Sarcoma, diffuse neonatal hemangiomatosis, familial glomangiomatosis, genetics of klippel-trenaunay-weber syndrome, maffucci syndrome and mucosal venous malformation syndrome.
Differentiating Blue rubber bleb nevus syndrome from other Diseases
Blue rubber bleb nevus syndrome must be differentiated from dermatologic manifestations of kaposi Sarcoma, diffuse neonatal hemangiomatosis, familial glomangiomatosis, genetics of klippel-trenaunay-weber syndrome, maffucci syndrome and mucosal venous malformation syndrome.
Disease | Symptoms | Physical examination | Lab Findings |
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Kaposi Sarcoma |
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Diffuse Neonatal Hemangiomatosis |
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Familial Glomangiomatosis[1] |
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biopsy | |
Genetics of Klippel-Trenaunay-Weber Syndrome |
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Maffucci Syndrome |
Blue rubber bleb nevus syndrome Microchapters |
Differentiating Blue Rubber Bleb Nevus Syndrome from other Diseases |
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Diagnosis |
Treatment |
Case Studies |
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