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- W2131990030 abstract "To the Editor: The vague clinical presentations of adrenal insufficiency (AI) in elderly patients could be considered to be due to the aging process, which would then be overlooked and become life threatening.1 It may be that the coexistence of AI and thyroid insufficiency, which may result from pituitary failure, is greater than previously suspected.2 An older man with hypothyroid secondary to subclinical hypopituitarism, in whom thyroid hormone replacement eventually resulted in adrenal crisis, is reported. A 79-year-old man was referred to the Department of Geriatric Gastroenterology PLA General Hospital, Beijing, China, in February 2010 because of intermittent diarrhea and constipation for 7 months. He had lost 5 kg of weight over this period. In 1979, he had received a 45-Gy dose of local irradiation to the pituitary area because of pituitary adenoma. Follow-up was every 1 to 2 years thereafter until 1993. He felt well and returned to normal work without taking hormone replacement. He presented elsewhere in 2007 with lassitude and intolerance to cold. Hypothyroidism was diagnosed, and levothyroxine was prescribed. He had a history of hypertension, coronary heart disease, multiple lacunar infarction, and cognitive impairment for years. The patient was brought into the ward in a wheelchair and confined to bed. Vital signs were normal. His facial appearance was dull and apathetic. A 4- × 3-cm abdominal mass was palpable at the lower right quadrant, with no tenderness. A few hyperpigmented patches were noted on the anterior tibial surfaces. The remainder of the examination was unremarkable. Hemoglobin was 10.8 g/dL (normocytic). Urine and stool examinations and chemistry panels were normal. Plasma carcinoembryonic antigen and carbohydrate antigen 72–4 were high. Low plasma thyroxine and triiodothyronine concentrations were recorded. Plasma thyroid-stimulating hormone (TSH) concentration was normal. The patient experienced hyponatremia (118 mEq/L) during bowel preparation for colonoscopy, but this was corrected with fluid resuscitation and sodium chloride supplementation. Levothyroxine dosage was increased to 37.5 μg daily, which resulted in normal plasma thyroxine concentrations. Thirty-five days later, he developed hypotension (90/60 mmHg) accompanied by rapid atrial fibrillation and sweating. Laboratory investigation showed serum sodium 131 mEq/L (130–150 mEq/L), potassium 4.3 mEq/L (3.5–5.5 mEq/L), and glucose 122 mg/dL (62–110 mg/dL). His symptoms were initially attributed to hypovolemia and tachyarrhythmia. Intravenous hydration and anti-arrhythmia drugs returned his blood pressure to normal. Hours later, his situation worsened with a systolic blood pressure of less than 60 mmHg. Hypopituitarism and adrenal crisis was suspected. Intravenous hydrocortisone (100 mg) was initiated immediately, which corrected the hypotensive episodes. He was then given 600 mg of hydrocortisone (100 mg every 4 hours) for 24 hours. Plasma adrenocorticotropic hormone levels tested the day after the attack at midnight, 8:00 a.m., and 4:00 p.m. were undetectable. Plasma prolactin, luteinizing hormone, and follicle-stimulating hormone concentrations were low. A diagnosis of hypopituitarism was made. Parenteral hydrocortisone was tapered over 2 weeks and changed to a maintenance dose of oral prednisone. A recent survey of patients with AI found that more than 67% consulted at least three physicians and that 68% were initially received the wrong diagnosis.3 Some patients initially present with gastrointestinal symptoms such as abdominal cramps, nausea, vomiting, and diarrhea.4 This patient presented with an irregular disturbance of defecation, a mass at the lower right quadrant, and high serum tumor marker levels. These characteristics led us to focus initially on gastrointestinal disorders. Comorbidities such as multiple lacunar infarction and cognitive dysfunction also led to a failure to notice the symptoms of lethargy and memory difficulties. The diagnosis of AI is frequently overlooked in inpatients with hyponatremia.5 Hyponatremia after bowel preparation in this case was considered to be one of the common complications of bowel cleansing in older adults and was thus neglected at the time. Adrenocorticotropic hormone and TSH deficiencies are more frequently described in patients with previous tumors or surgical insults to the pituitary gland.6 This patient presented a TSH deficiency 28 years after radiation, which was longer than other similar reports documented. Primary hypopituitarism is not uncommon in older adults.7 Aging and radiation might have both contributed to his hypopituitarism. Although it is widely recognized that thyroid hormone precipitates adrenal crisis, few cases have been reported in the literature.8 In this case, the normal TSH level led to a delay in the recognition of accompanying pituitary failure. Apparently, he had subclinical AI when levothyroxine was initially prescribed, which became clinically manifest when the thyroxine dose was raised. Elderly patients should not be started on thyroxine replacement therapy until the possibility of hypopituitarism and adrenal deficiency has been excluded. Conflict of Interest: The editor in chief has reviewed the conflict of interest checklist provided by the authors and has determined that the authors have no financial or any other kind of personal conflicts with this paper. Author Contributions: GS Wang contributed to the conception and design, acquisition of data and preparation of the article. CH Cai and BY Wu revised for important intellectual content. All authors meet the criteria for authorship stated in the Uniform Requirements for Manuscripts Submitted to Biomedical Journals. The authors had a final approval of the version to be published. Sponsor's Role: NA." @default.
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- W2131990030 date "2010-12-01" @default.
- W2131990030 modified "2023-10-18" @default.
- W2131990030 title "THYROID HORMONES PRECIPITATE SUBCLINICAL HYPOPITUITARISM RESULTED IN ADRENAL CRISIS" @default.
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- W2131990030 doi "https://doi.org/10.1111/j.1532-5415.2010.03188.x" @default.
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