1.
Pediatr Dermatol
; 34(3): e128-e129, 2017 May.
Article
in English
| MEDLINE
| ID: mdl-28318049
ABSTRACT
We describe the case of a 33-week preterm infant who developed nonimmune hydrops fetalis secondary to a kaposiform hemangioendothelioma (KHE). The tumor was successfully treated with vincristine, prednisone, ticlopidine, and aspirin. KHE can be an unusual cause of hydrops fetalis; in such cases, diagnosis can be challenging since generalized edema can obscure KHE.
Subject(s)
Hemangioendothelioma/diagnostic imaging , Hemangioendothelioma/drug therapy , Hydrops Fetalis/diagnosis , Infant, Premature , Kasabach-Merritt Syndrome/diagnostic imaging , Kasabach-Merritt Syndrome/drug therapy , Magnetic Resonance Imaging/methods , Sarcoma, Kaposi/diagnostic imaging , Sarcoma, Kaposi/drug therapy , Vincristine/administration & dosage , Administration, Oral , Aspirin/administration & dosage , Cesarean Section , Diagnosis, Differential , Drug Therapy, Combination , Follow-Up Studies , Gestational Age , Hemangioendothelioma/diagnosis , Humans , Hydrops Fetalis/diagnostic imaging , Infusions, Intravenous , Kasabach-Merritt Syndrome/diagnosis , Male , Prednisone/administration & dosage , Sarcoma, Kaposi/diagnosis , Ticlopidine/administration & dosage , Treatment Outcome
2.
Rev. neurol. (Ed. impr.)
; 59(5): 238-240, 1 sept., 2014. ilus, tab
Article
in Spanish
| IBECS
| ID: ibc-126277
ABSTRACT
No disponible
Subject(s)
Humans , Male , Child, Preschool , Muscular Dystrophies/diagnosis , Magnetic Resonance Spectroscopy , Diagnosis, Differential , Muscular Dystrophy, Emery-Dreifuss/diagnosis
3.
Rev Neurol
; 59(5): 238-40, 2014 Sep 01.
Article
in Spanish
| MEDLINE
| ID: mdl-25156028