Paul's
Panhypopituitarism was caused by a birth defect which left him with a piece of his skull missing.
He also has a rare condition called
panhypopituitarism where his pituitary gland is suffering complete failure.
The patient was born at 32 weeks' gestation with subsequent developmental delay, agenesis of the corpus callosum, and
panhypopituitarism.
Panhypopituitarism secondary to pituitary metastases.
Common Pediatric Factors Affecting Male Fertility Chromosomal Klinefelter syndrome Kallman syndrome Noonan syndrome Absence of vas deferens Structural Varicocele Undescended testes Metabolic Growth hormone deficiency
Panhypopituitarism Illicit Drug Use Marijuana, cocaine, smoking Anabolic steroid abuse Traumatic Testicular torsion Trauma Iatrogenic Chemotherapy Local radiation Infectious Mumps orchitis Epidydimitis Table 2.
Lliam suffers from a rare condition known as congenital
panhypopituitarism, as well as septo optic dysplasia, which both result in him having an adrenal insufficiency.
CNS tuberculomas can have varied clinical presentation ranging from mild headache, convulsions, hemiplegia, and also few rare presentations like
panhypopituitarism (6), unilateral or bilateral internuclear ophthalmoplegia, "one and a half" syndrome, and "eight and a half" syndrome have also been reported.
The patient subsequently developed
panhypopituitarism, diabetes insipidus and total blindness.
Severe cases with extensive invasion can exhibit the full-blown hypothalamic syndrome with morbid obesity, temperature and sleep disorders,
panhypopituitarism, and seizures.
Both these patients had a history of
panhypopituitarism and were prescribed chronic hormone replacement therapy.
Presentations of above cases approximately were
panhypopituitarism or visual disturbances, similar our patient had chronic headache and hyperprolactemia with visual field defects.
As the pituitary parenchyma is destroyed by the inflammatory process, partial or
panhypopituitarism develops.