Retinal vaso occlusion in sickling hemoglobinopathies

Research output: Contribution to journalArticle

Abstract

Sickle cell retinopathy, in all of its manifestations, represents the effects of arteriolar and capillary occlusions. Increased viscosity of circulating whole blood plus the microembolic action of individual sickled erythrocytes contribute to vaso occlusion. Decreased oxygenation and increased acidosis develop and lead to further sickling, and further vaso occlusion. The cycle of erythrostasis that characterizes sickling throughout the body is also applicable to the retina. The transparent media of the eye permit direct visualization of vaso occlusions which occur preferentially in and about the macula and in the far periphery of the retina. Many of the occlusive episodes are transient. These dynamic events are simultaneously occurring elsewhere in the body but can only be visualized in the eye. The net effect in the retina is a remodeling of its vasculature, as some vessels close and other reopen. After the onset of arteriolar closure in the retina, affected blood vessels embark on a spontaneous, naturally evolving course of events leading to arteriolar venular anastomoses, neovascular proliferations, vitreous hemorrhages, and retinal detachment. The advanced stages of proliferative sickle retinopathy are most commonly observed in SC disease and in Sthal, possibly because these two forms of sickling have significantly higher than normal blood viscosity. Retinal vaso occlusions can also lead to blow out hemorrhages which may evolve into salmon patches, irridescent spots, schisis cavities, and black sunbursts. In some respects sickle retinopathy is unique, but many of its manifestations are similar to those of retinopathies found in diabetes mellitus, AC hemoglobinopathy, Takayasu pulseless disease, sarcoidosis, chronic myelogenous leukemia, branch retinal vein occlusion, retrolental fibroplasia, and Eales disease.

Original languageEnglish (US)
Pages (from-to)475-515
Number of pages41
JournalBirth Defects: Original Article Series
Volume12
Issue number3
StatePublished - 1976
Externally publishedYes

Fingerprint

Hemoglobinopathies
Retina
Takayasu Arteritis
Hemoglobin SC Disease
Vitreous Detachment
Vitreous Hemorrhage
Retinal Vein Occlusion
Retinopathy of Prematurity
Blood Viscosity
Salmon
Retinal Detachment
Sarcoidosis
Leukemia, Myelogenous, Chronic, BCR-ABL Positive
Acidosis
Viscosity
Blood Vessels
Diabetes Mellitus
Erythrocytes
Hemorrhage

ASJC Scopus subject areas

  • Developmental Biology
  • Genetics(clinical)

Cite this

Retinal vaso occlusion in sickling hemoglobinopathies. / Goldberg, Morton F.

In: Birth Defects: Original Article Series, Vol. 12, No. 3, 1976, p. 475-515.

Research output: Contribution to journalArticle

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