Ophthalmology · MU Sofia

68. Retinal detachment - types, clinical findings and treatment

Covers retinal detachment, separating the rhegmatogenous, tractional, exudative, tumour-related and falciform forms, then listing symptoms, signs, risk factors, diagnosis by ophthalmoscopy and surgical and laser treatment options. It then moves to retinoblastoma, covering its epidemiology, heritability, clinical signs, imaging comparison of ultrasound, CT and MRI, differential diagnoses and treatment by tumour size.

Inside: 1 section · 6 labelled pictures · 14 flashcards · 4 min

Topic 68 of 91 in the MU Sofia syllabus for Ophthalmology (Medicine, Year 4). The free AceMed note covers it in 1 section, about 541 words (4 min of reading), with 14 flashcards.

In this note

  1. Retinal detachment. Retinoblastoma

Retinal detachment. Retinoblastoma

Retinal detachment = Displacement of the neurosensory retina from the retinal pigment epithelium

Retinal detachment (Amotio retinae) refers to the detachment of the inner layer of the retina (neurosensory part) from its base, the retinal pigment epithelium. This leads to a loss of function in the lifted portion and to corresponding visual field defects. The most common cause of retinal detachments are cracks or holes in the retina, which can be caused by a glass body lift, for example. To prevent retinal detachment, circular laser coagulation in the immediate vicinity of the retinal defect should be performed when retinal tears or holes are diagnosed. Retinal detachment is an ophthalmological emergency and usually needs to be surgically treated promptly to prevent further detachment of the retina and restore sensory function as much as possible. The prognosis for vision depends mainly on the extent of the amotio (poor in macular involvement) and the length of time until the retina is restored.

Etiology:

Forms of retinal detachment

  • Rhegmatogen (due to cracks): most common form, e.g. in the context of an acute, posterior vitreous detachment or traumatic
  • Tractional
  • Symptoms :
  • Photopsia and floaters are absent, visual field defects progress slowly
  • Signs:
  • Detached retina is concave and breaks are absent, retinal mobility is severely reduced, shifting fluid is absent
  • Exudative (due to fluid)
  • Caused by a tumor
  • Special forms: Falciform (in persistent hyperplastic primary vitreous)

Pathoyphsiology:

  • Detachment of the retina by submerging the retina with fluid
  • Functional loss of the retina due to impaired metabolic processes

Symptoms of rhegmatogenous retinal detachment:

  • Visual field defects
  • Flashes of light (photopsias)
  • Black spots in the vitreous body due to intravitreal bleeding
  • Distorted vision
  • Floaters

Signs:

  • The detached retina has a convex configuration
  • Slightly opaque and corrugated appearance
  • Undulates freely with eye movements
  • Retinal breaks
  • RAPD
  • ↓ IOP

Risk factors of rhegmatogenous form:

  • Myopia
  • Vitreous detachment
  • Traumata (Bulbus Contusion)
  • Condition after retinal detachment of the other eye
  • Family stress
  • Condition after cataract surgery

Diagnosis: Ophthalmoscopy

Therapy:

If there are retinal holes or tears and very little local retinal detachment:

  • Circular (argon) laser coagulation in the immediate vicinity of the retinal defect

For more extensive retinal detachment:

  • Surgical procedure
  • Denting procedures
  • Cryotherapy
  • Replacement of the vitreous

Retinoblastoma:

  • The most common primary intraocular tumor in childhood
  • Occurring in about 1:20 000 live births - 3% of all childhood cancers

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