Blue rubber bleb nevus syndrome differential diagnosis: Difference between revisions

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* Painful [[cutaneous]] lesions
* Painful [[cutaneous]] lesions
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* Painful [[cutaneous]] lesions
* Lesions that:
** looks like plaque
** looks like cobblestone
** Hyperkeratotic, dark blue or purple lesions  
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|
* Biopsy
* Biopsy shows the following:<ref name="pmid118454072">{{cite journal |vauthors=Brouillard P, Boon LM, Mulliken JB, Enjolras O, Ghassibé M, Warman ML, Tan OT, Olsen BR, Vikkula M |title=Mutations in a novel factor, glomulin, are responsible for glomuvenous malformations ("glomangiomas") |journal=Am. J. Hum. Genet. |volume=70 |issue=4 |pages=866–74 |date=April 2002 |pmid=11845407 |pmc=379115 |doi=10.1086/339492 |url=}}</ref>
** Undifferentiated smooth muscle cells surrounding convoluted venous channels
|-
|-
|Genetics of Klippel-Trenaunay-Weber Syndrome
|Genetics of Klippel-Trenaunay-Weber Syndrome

Revision as of 17:57, 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
Kaposi Sarcoma
Diffuse Neonatal Hemangiomatosis
  • Difficulty in walking
  • Radiologic evaluation is very important in the follow of Diffuse Neonatal Hemangiomatosis which shows the following
    • Destruction of cortex
    • Endosteal cortical erosion
    • Zones of lucency
Familial Glomangiomatosis[1]
  • Lesions that:
    • looks like plaque
    • looks like cobblestone
    • Hyperkeratotic, dark blue or purple lesions
  • Biopsy shows the following:[2]
    • Undifferentiated smooth muscle cells surrounding convoluted venous channels
Genetics of Klippel-Trenaunay-Weber Syndrome
Maffucci Syndrome

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References

  1. Iqbal A, Cormack GC, Scerri G (January 1998). "Hereditary multiple glomangiomas". Br J Plast Surg. 51 (1): 32–7. PMID 9577316.
  2. 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.

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