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신경외과/Tumor

Pituitary tumors & Hemangioblastoma

by 혀ni 2021. 6. 8.
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Sellar anatomy

Diseases related to hypothalamic-pituitary axis

  • Neoplastic disorders

    Pituitary adenoma, craniopharyngioma, germinoma and teratoid tumor, hypothalamic and optic glioma,   
    meningioma

  • Non-neoplastic cystic lesions

    Rathke’s cleft cyst, mucocele, arachnoid cyst, epidermoid cyst

  • Inflammatory disorders

    Pituitary abscess, lymphocytic hypophysitis

  • Head trauma

    Basal skull fracture, severe cerebral contusion

 

 

Pituitary adenoma

  • Benign tumor arising pituitary gland

    4-5th decades, female>male

  • Classification according to hormonal secretion

    Non-functioning (hormone non-secreting): 15~30%

    Functioning (hormone secreting): 48% prolactin, 10% GH, 6% ACTH, 1% TSH

  • Classification according to tumor size
  1. Micro-adenoma ( < 1 cm)
  2. Macro-adenoma ( >1 cm)
  3. Giant adenoma  ( > 4 cm)

 

Non-functioning pituitary adenoma

  • Sx & Sn by mass effect

    Visual manifestations: impairment of visual acuity, visual field defect

     bitemporal hemianopsia due to optic chiasm compression

    Cranial nerve palsies : EOM (extra-ocular muscle) limitations, facial numbness & pain

    Headache

    Obstructive hydrocephalus: foramen of Monro, 3rd ventricle

    Pseudo-hyperprolactinemia (<150 ng/mL) due to stalk compression effect

    Hypopituitarism: later stage (Go Look For The Adenoma, Please!)

    Diabetes insipidus

Table 44.3 Significance of prolactin levelsa
PRL (ng/ml) Interpretation Situations observed in
3–30b normal non-pregnant female
10–400 pregnancy
2–20 postmenopausal female
25b-150 moderate elevation prolactinoma
“stalk effect” (see text)
other causesd
> 150c significant elevation prolactinomad
Note: ectopic sites of prolactin secretion have rarely been reported (e.g. in a teratoma)
normal values vary, use your lab’s reference range 
some authors recommend 200 ng/ml as the cutoff for probable prolactinomas14 d for DDx of hyperprolactinemia

 

Hemangioblastoma

Table 41.5 Associations with von Hippel-Lindau disease
Common lesions Frequency in VHL
hemangioblastomas
cerebellum (solid or cystic) 80%
retina 41–59%
brainstem 10–25%
spinal cord 10–50%
pancreatic tumors or cysts 22–80%
renal clear cell Ca & cysts 14–60%
polycythemia 9–20% of intracranial HGBs
Rare lesions (pertinent to nervous system) Frequency in VHL
supratentorial hemangioblastoma 3–6%
cystadenomas of the broad ligament 10% of
papillary cystadenomas of epididymis 25–60%
endolymphatic sac tumors 10–15%
adrenal medullary pheochromocytoma (tends to be bilateral) 7–24%
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