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What is Panhypopituitarism

Panhypopituitarism description. Find out what Panhypopituitarism is and know more about it.

What is Panhypopituitarism

Panhypopituitarism is a rare disorder characterized by the underproduction or complete absence of hormones secreted by the pituitary gland. The pituitary gland, often referred to as the "master gland," is responsible for producing and regulating several essential hormones that control various bodily functions.



Panhypopituitarism can occur due to different causes, including tumors, genetic abnormalities, infections, or traumatic brain injuries affecting the pituitary gland. The condition leads to a deficiency in multiple hormones, such as growth hormone, thyroid-stimulating hormone, adrenocorticotropic hormone, follicle-stimulating hormone, luteinizing hormone, and prolactin.



Signs and symptoms of panhypopituitarism can vary depending on which hormones are affected, but commonly include fatigue, weight loss, decreased libido, infertility, low blood pressure, and intolerance to stress or cold temperatures. Prompt diagnosis is crucial as untreated panhypopituitarism can lead to serious complications.



Treatment for panhypopituitarism typically involves hormone replacement therapy to restore the deficient hormones. Patients may require lifelong treatment and regular monitoring to ensure hormone levels are adequately maintained. Additionally, addressing the underlying cause, such as surgery or radiation therapy for tumors, may be necessary.


Diseasemaps
2 answers
Panhypopituitarism is a potentially life-threatening endocrine disorder that is classified by a distinct absence of pituitary hormones, which, consequently, causes hormone insufficiencies in the other endocrine glands, most notably, the thyroid, adrenals, and ovaries/testes due to the pituitary being unable to release the hormones necessary to trigger the function of these target glands. This dangerous domino effect, then, is what leads to the rise of the symptoms we face every day and the reason why we take our medicine and need constant blood work and appointments etc.

Posted Dec 7, 2018 by Ty 4960

What is Panhypopituitarism

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ICD9 and ICD10 codes of Panhypopituitarism

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World map of Panhypopituitarism

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Stories of Panhypopituitarism

PANHYPOPITUITARISM STORIES
Panhypopituitarism stories
Пангипопитуитаризм возник вследствии опухоли гипофиза- краниофарингиомы, нет все гомонов гипофиза, гипофиза тоже нет
Panhypopituitarism stories
In September of 2013 I started to have prolonged headaches. I went to several doctors and a chiropractor but no one seemed to know why I was having headaches. I finally went to the ER and after dealing with initial looks of dismissal as to why I woul...
Panhypopituitarism stories
Mum to congenital pan-hypit girl
Panhypopituitarism stories
I was Born with PHP. I wasn't properly diagnosed until I was 3. 
Panhypopituitarism stories
A few doctors theorized my pregnancy caused a macro adenoma. I began having weird symptoms before I was diagnosed i.e. My hair started falling out, my nails began to pit, I had galactorrhea even though I quit nursing a year before, no menses, and I s...

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Panhypopituitarism forum

PANHYPOPITUITARISM FORUM
Panhypopituitarism forum
Even though I am taking typically 35mg of Hydrocortisone, 20 at 8 am, 10 at 11 am and 5 at 2pm I suffer from sensitivity to glare and feel light headed and dizzy. it is hard to concentrate and generally feel crook. I am on Testesterone gel, 1 sachet...
Panhypopituitarism forum
My 22-year-old nephew was diagnosed with panhypopituitarism before he was one year old. He's taken Cortef, growth hormone, and Synthroid since then. The last few years he's had problems with social anxieties and depression. He's done a lot of jumping...

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