Blue rubber bleb nevus syndrome differential diagnosis: Difference between revisions
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!'''Lab Findings''' | !'''Lab Findings''' | ||
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|Kaposi Sarcoma | |Kaposi Sarcoma<ref name="pmid8880194">{{cite journal |vauthors=Dezube BJ |title=Clinical presentation and natural history of AIDS--related Kaposi's sarcoma |journal=Hematol. Oncol. Clin. North Am. |volume=10 |issue=5 |pages=1023–9 |date=October 1996 |pmid=8880194 |doi= |url=}}</ref> | ||
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* [[Fever]] | * [[Fever]] | ||
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* The color of the [[lesions]] may change into blue, purple, or brown as the disease progress | * The color of the [[lesions]] may change into blue, purple, or brown as the disease progress | ||
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* CD4+ T-lymphocyte count | |||
* Decreased [[hemoglobin]] level | * Decreased [[hemoglobin]] level | ||
* [[Antibodies]] against KSHV | * [[Antibodies]] against KSHV | ||
* CD34, [[HHV-8]], and D2-40 positive | * CD34, [[HHV-8]], and D2-40 positive | ||
* [[Fecal occult blood test]] | |||
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|Diffuse Neonatal Hemangiomatosis | |Diffuse Neonatal Hemangiomatosis | ||
Revision as of 14:11, 7 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 |
|---|---|---|---|
| Kaposi Sarcoma[1] |
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| Diffuse Neonatal Hemangiomatosis |
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| Familial Glomangiomatosis[2] |
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| Genetics of Klippel-Trenaunay-Weber Syndrome |
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| Maffucci Syndrome[5][6] |
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Blue rubber bleb nevus syndrome Microchapters |
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Differentiating Blue Rubber Bleb Nevus Syndrome from other Diseases |
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Diagnosis |
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Treatment |
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References
- ↑ Dezube BJ (October 1996). "Clinical presentation and natural history of AIDS--related Kaposi's sarcoma". Hematol. Oncol. Clin. North Am. 10 (5): 1023–9. PMID 8880194.
- ↑ Iqbal A, Cormack GC, Scerri G (January 1998). "Hereditary multiple glomangiomas". Br J Plast Surg. 51 (1): 32–7. PMID 9577316.
- ↑ Boon LM, Mulliken JB, Enjolras O, Vikkula M (August 2004). "Glomuvenous malformation (glomangioma) and venous malformation: distinct clinicopathologic and genetic entities". Arch Dermatol. 140 (8): 971–6. doi:10.1001/archderm.140.8.971. PMID 15313813.
- ↑ Brouillard P, Boon LM, Mulliken JB, Enjolras O, Ghassibé M, Warman ML, Tan OT, Olsen BR, Vikkula M (April 2002). "Mutations in a novel factor, glomulin, are responsible for glomuvenous malformations ("glomangiomas")". Am. J. Hum. Genet. 70 (4): 866–74. doi:10.1086/339492. PMC 379115. PMID 11845407.
- ↑ Enjolras O, Wassef M, Merland JJ (August 1998). "[Maffucci syndrome: a false venous malformation? A case with hemangioendothelioma with fusiform cells]". Ann Dermatol Venereol (in French). 125 (8): 512–5. PMID 9747318.
- ↑ Schwartz HS, Zimmerman NB, Simon MA, Wroble RR, Millar EA, Bonfiglio M (February 1987). "The malignant potential of enchondromatosis". J Bone Joint Surg Am. 69 (2): 269–74. PMID 3805090.
- ↑ Pansuriya TC, Kroon HM, Bovée JV (June 2010). "Enchondromatosis: insights on the different subtypes". Int J Clin Exp Pathol. 3 (6): 557–69. PMID 20661403.