Tuberous Sclerosis Flashcards

1
Q

Tuberous Sclerosis

A

This patient has had a first seizure recently. Please examine them as you wish. What is the diagnosis?

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2
Q

Clinical signs of Tuberous sclerosis

A
  1. Skin changes
  2. Respiratory
  3. Abdominal
  4. Eyes
  5. CNS
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3
Q

Clinical signs: Skin changes

A
  1. Facial (perinasal: butterfly distribution) adenoma sebaceum (angiofibromata)
  2. Periungual fibromas (hands and feet)
  3. Shagreen patch: roughened, leathery skin over the lumbar region
  4. Ash leaf macules: depigmented macules on trunk (fluoresce with UV/Wood’s light)
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4
Q

Clinical signs: Respiratory

A
  • Cystic lung disease
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5
Q

Clinical signs: Abdominal

A
  1. Renal enlargement caused by polycystic kidneys and/or renal angiomyolipomata
  2. Transplanted kidney
  3. Dialysis fistulae
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6
Q

Clinical Signs: Eyes

A
  • Retinal phakomas (dense white patches) in 50%
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7
Q

Clinical signs: CNS

A
  1. Mental retardation may occur
  2. Seizures
  3. Signs of anti‐epileptic treatment, e.g. phenytoin: gum hypertrophy and hirsuitism
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8
Q

Mnemonic in Tuberous sclerosis

A

Previously known as EPILOIA (EPIlepsy, LOw Intelligence, Adenoma sebaceum)

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9
Q

Tuberous sclerosis Mnemonic 1st Aid

A

HAMARTOMAS:
Hamartomas in CNS and skin;
Angiofibromas;
Mitral regurgitation;
Ash-leaf spots;
cardiac Rhabdomyoma;
(Tuberous sclerosis);
autOsOmal dOminant;
Mental retardation (intellectual disability);
renal Angiomyolipoma;
Seizures, Shagreen patches.

Incidence of subependymal astrocytomas and ungual fibromas.

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10
Q

Discussion of Tuberous sclerosis

A
  • Autosomal dominant (TSC1 on chromosome 9, TSC2 on chromosome 16) with variable penetrance
  • 80% have epilepsy (majority present in childhood; but adult presentation also seen)
  • Cognitive defects in 50%
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11
Q

Renal manifestations in Tuberous sclerosis

A
  1. Renal angiomyolipomas, renal cysts and renal cell carcinoma
  2. The genes for tuberous sclerosis and ADPKD are contiguous on chromosome 16, hence some mutations lead to both conditions
  3. Renal failure may result from cystic disease, or parenchymal destruction by massive angiomyolipomas
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12
Q

Investigation for Tuberous sclerosis

A
  1. Skull films: ‘railroad track’ calcification
  2. CT/MRI head: tuberous masses in cerebral cortex (often calcify)
  3. Echo and abdominal ultrasound: hamartomas and renal cysts
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