Ms. Guoth et al., NEUROSARCOIDOSIS PRESENTING AS HYPOPITUITARISM AND A CYSTIC PITUITARYMASS, The American journal of the medical sciences, 315(3), 1998, pp. 220-224
We report a young woman with clinical hypopituitarism and systemic sar
coidosis involving the lung, gastrointestinal tract, and peripheral ly
mph nodes, Laboratory evaluation confirmed that cortisol, thyroid indi
ces, insulin-like growth factor 1, follicle-stimulating hormone, lutei
nizing hormone, and estradiol levels were low, with a normal prolactin
, Magnetic resonance imaging revealed a large cystic pituitary lesion
compressing the optic chiasm and exhibiting rim but not hypothalamic e
nhancement, The differential diagnosis included cystic macroadenoma, R
athke's cleft cyst, craniopharyngioma, and simple cyst, A transsphenoi
dal procedure provided decompression and diagnosis: pathology was cons
istent with sarcoidosis, Postoperatively, the patient's neurosarcoid d
isease markedly worsened, requiring hypothalamic irradiation, To our k
nowledge, this is the first report of intracranial sarcoidosis present
ing solely as a cystic pituitary mass. An awareness of this possibilit
y is important to prevent inappropriate neurosurgical intervention and
subsequent potential exacerbation of neurosarcoidosis.