Neurocutaneous melanosis: definition and review of the literature.
Aplasia cutis congenita: a clinical review and proposal for classification.
- I. Frieden
- MedicineJournal of American Academy of Dermatology
- 1 April 1986
PHACE syndrome. The association of posterior fossa brain malformations, hemangiomas, arterial anomalies, coarctation of the aorta and cardiac defects, and eye abnormalities.
The acronym PHACE syndrome is proposed to emphasize the characteristic findings of this neurocutaneous syndrome: posterior fossa malformations, hemangiomas, arterial anomalies, coarctation of the aorta and cardiac defects, and eye abnormalities.
Vascular Anomalies Classification: Recommendations From the International Society for the Study of Vascular Anomalies
The updated official ISSVA classification of vascular anomalies is presented, acknowledging that it will require modification as new scientific information becomes available.
Vascular malformations: Part I.
Initiation and Use of Propranolol for Infantile Hemangioma: Report of a Consensus Conference
The multidisciplinary team agreed on a number of recommendations that arose from a review of existing evidence, including when to treat complicated IH; contraindications and pretreatment evaluation protocols; propranolol use in PHACE syndrome; formulation, target dose, and frequency of proPRanolol; initiation of propr ethanol in infants; cardiovascular monitoring; ongoing monitoring; and prevention of hypoglycemia.
Prospective Study of Infantile Hemangiomas: Clinical Characteristics Predicting Complications and Treatment
Large size, facial location, and/or segmental morphology are the most important predictors of poor short-term outcomes as measured by complication and treatment rates in infantile hemangiomas.
Parkes Weber syndrome, vein of Galen aneurysmal malformation, and other fast‐flow vascular anomalies are caused by RASA1 mutations
This first extensive study on the phenotypes associated with RASA1 mutations, and unravels their wide heterogeneity is reported, finding some CM‐AVM patients had neural tumors reminiscent of neurofibromatosis type 1 or 2.
Mycoplasma pneumoniae-induced rash and mucositis as a syndrome distinct from Stevens-Johnson syndrome and erythema multiforme: a systematic review.
Hemangiomas of infancy: clinical characteristics, morphologic subtypes, and their relationship to race, ethnicity, and sex.
Hemangiomas of infancy can usually be classified as localized, segmental, indeterminate, and multifocal, but this type of hemangioma seems to present with increased frequency in Hispanic infants.