1.Hemophagocytic Syndrome Associated with Bilateral Adrenal Gland Tuberculosis.
Byung Chul SHIN ; Shin Woo KIM ; Sang Woo HA ; Jong Won SOHN ; Jong Myung LEE ; Nung Soo KIM
The Korean Journal of Internal Medicine 2004;19(1):70-73
We report a case of a patient who presented with hemophagocytic syndrome (HPS) and adrenal crisis associated with bilateral adrenal gland tuberculosis, and resulted in a poor outcome. A 50-year-old man was transferred to our hospital from a local clinic due to fever, weight loss, and bilateral adrenal masses. Laboratory findings showed leukopenia, mild anemia, and elevated lactate dehydrogenase. Computed tomography (CT) of the abdomen revealed bilateral adrenal masses and hepatosplenomegaly. CT-guided adrenal gland biopsy showed numerous epithelioid cells and infiltration with caseous necrosis consistent with tuberculosis. Bone marrow aspiration and biopsy showed significant hemophagocytosis without evidence of malignancy, hence HPS associated with bilateral adrenal tuberculosis was diagnosed. During anti-tuberculosis treatment the patient showed recurrent hypoglycemia and hypotension. Rapid ACTH stimulation test revealed adrenal insufficiency, and we added corticosteroid treatment. But pancytopenia, especially thrombocytopenia, persisted and repeated bone marrow aspiration showed continued hemophagocytosis. On treatment day 41 multiple organ failure occurred in the patient during anti-tuberculous treatment and steroid replacement.
Adrenal Gland Diseases/*complications/drug therapy/radiography
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Antitubercular Agents/therapeutic use
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Histiocytosis, Non-Langerhans-Cell/*etiology/pathology
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Human
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Isoniazid/therapeutic use
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Male
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Middle Aged
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Tomography, X-Ray Computed
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Tuberculosis, Endocrine/*complications/drug therapy/radiography
2.A case of adrenal gland dependent hyperadrenocorticism with mitotane therapy in a Yorkshire terrier dog.
Young Mi LEE ; Byeong Teck KANG ; Dong in JUNG ; Chul PARK ; Ha Jung KIM ; Ju Won KIM ; Chae Young LIM ; Eun Hee PARK ; Hee Myung PARK
Journal of Veterinary Science 2005;6(4):363-366
Hyperadrenocorticism, a disorder characterized by excessive production of cortisol by the adrenal cortex, is wellrecognized in dogs. A 10-year-old, intact male, Yorkshire terrier dog was evaluated because of corneal ulceration and generalized alopecia. Diagnosis was made based on history taking, clinical signs, physical examination, and results of routine laboratory testing (complete blood count, serum biochemical analysis, and urinalysis). In addition, adrenocorticotropic hormone (ACTH) stimulation test and abdominal ultrasonography were also used to diagnose this case. The patient was diagnosed as adrenal gland neoplasia and medical therapy using the adrenocorticolytic agent, mitotane, was initiated. An ACTH stimulation test was performed after initial therapy. After successful induction was obtained, maintenance therapy with mitotane still continued.
Adrenal Gland Neoplasms/complications/diagnosis/drug therapy/*veterinary
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Adrenocortical Hyperfunction/diagnosis/drug therapy/etiology/*veterinary
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Adrenocorticotropic Hormone/blood
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Animals
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Antineoplastic Agents, Hormonal/*therapeutic use
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Dog Diseases/*drug therapy
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Dogs
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Male
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Mitotane/*therapeutic use
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Radiography, Abdominal/veterinary
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Tomography, X-Ray/veterinary