Abstract
We describe the clinical and pathologic features of an unusual case of alpha-thalassemia major in a patient who survived to term and lived for 9 days. The neonate was nonhydropic and the clinical picture was dominated by severe hypoxia with pulmonary hypertension. The diagnosis was not suspected until postnatal examination of the blood smear, which prompted the performance of hemoglobin electrophoresis and subsequent molecular confirmation. This case illustrates that alpha-thalassemia major should be in the differential diagnosis of hypoxic neonates even in the absence of hydrops.
Original language | English (US) |
---|---|
Pages (from-to) | 706-709 |
Number of pages | 4 |
Journal | Pediatric and Developmental Pathology |
Volume | 8 |
Issue number | 6 |
DOIs | |
State | Published - Dec 2005 |
Externally published | Yes |
Keywords
- Alpha-thalassemia major
- Hemoglobin Bart
- Hydrops fetalis
- Thalassemia
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health
- Pathology and Forensic Medicine