Isolated ACTH deficiency in self referred patients for LOH syndrome: two case reports

• Published in: Reproductive medicine and biology 2012-07, Vol.11 (3), p.155-158
• Main Authors: Sato, Yoshikazu, Tanda, Hitoshi, Nakajima, Hisao, Nitta, Toshikazu, Akagashi, Keigo, Hanzawa, Tatsuo, Tobe, Musashi, Haga, Kazunori, Uchida, Kousuke, Honma, Ichiya
• Format: Article
• Language: English
• Subjects: Adrenal insufficiency; Adrenocorticotropic hormone; Appetite loss; Case Report; Case reports; Differential diagnosis; General malaise; Gynecology; Hypogonadism; Hypotension; Isolated ACTH deficiency; LOH syndrome; Medicine; Medicine & Public Health; Reproductive Medicine; Urology
• ISSN: 1445-5781; 1447-0578
• DOI: 10.1007/s12522-012-0121-1

We experienced two cases of isolated ACTH deficiency (IAD) in patients self referred for late-onset hypogonadism (LOH) syndrome. IAD is secondary adrenal insufficiency due to lack of secretion of ACTH and delayed diagnosis of this rare condition may be life-threatening. The predominant symptoms of IAD, such as general malaise and weakness, resemble those of LOH syndrome creating the possibility that IAD may be referred as LOH syndrome. Two middle aged men with severe general malaise visited our clinic requesting evaluation for LOH syndrome. Previous treatments had been ineffective and based on varying incorrect diagnoses by previous doctors. The patients self referred themselves for LOH syndrome. Some of their symptoms were consistent with LOH syndrome but others were atypical, in particular, the severity of malaise and appetite loss. Hormonal assays were compatible with adrenal insufficiency secondary to ACTH deficiency. Steroid replacement dramatically improved their symptoms. The clinical course of our two patients and points of differential diagnosis between IAD and LOH syndrome are reported here.