期刊论文详细信息
Journal of Medical Case Reports
Isolated adrenocorticotropic hormone deficiency development during chemotherapy for gastric cancer: a case report
Tetsuo Ohta1  Takashi Fujimura1  Hirohisa Kitagawa1  Itasu Ninomiya1  Hiroyuki Takamura1  Keishi Nakamura1  Koichi Okamoto1  Toshifumi Watanabe1  Katsunobu Oyama1  Sachio Fushida1  Shinnosuke Higashino1  Jun Kinoshita1 
[1] Department of Gastroenterologic Surgery, Division of Cancer Medicine, Graduate School of Medical Science, Kanazawa University, 13-1 Takaramachi, Kanazawa 920-8641, Japan
关键词: Isolated ACTH deficiency;    Hyponatremia;    Gastric cancer;    Chemotherapy;   
Others  :  822565
DOI  :  10.1186/1752-1947-8-90
 received in 2013-12-01, accepted in 2014-01-09,  发布年份 2014
PDF
【 摘 要 】

Introduction

Isolated adrenocorticotropic hormone deficiency is an endocrinological disorder characterized by loss of adrenocorticotropic hormone and resultant adrenal insufficiency. Affected patients often present with fatigue, anorexia, and hyponatremia. Although the number of reported cases has been recently increasing, isolated adrenocorticotropic hormone deficiency combined with malignant neoplasia is very rare. Here we describe a patient with gastric cancer who developed unexpected isolated adrenocorticotropic hormone deficiency during chemotherapy.

Case presentation

A 72-year-old Japanese man was admitted to our hospital because of febrile neutropenia due to chemotherapy for gastric cancer recurrence. Although the neutropenia and fever immediately improved, he became unable to take any oral medications and was bedridden 1 week after admission. His serum sodium level abruptly decreased to 122mEq/L on the fifth day of hospitalization. We performed endocrinological studies to investigate the cause of his hyponatremia and plasma hyposmolality. His plasma adrenocorticotropic hormone and cortisol levels were very low. However, his serum levels of all other anterior pituitary hormones were slightly elevated. We then performed a corticotropin-releasing hormone test, which showed that neither his plasma adrenocorticotropic hormone nor cortisol level responded to corticotropin-releasing hormone stimulation. We definitively diagnosed isolated adrenocorticotropic hormone deficiency based on these findings. Hydrocortisone replacement therapy was begun at 20mg/day, resulting in a marked improvement in his anorexia and general fatigue within a few days. His serum sodium level was also normalized immediately after the administration of hydrocortisone. He was discharged from our hospital on the 50th day of hospitalization.

Conclusions

The present case is the second report of a patient with concurrent isolated adrenocorticotropic hormone deficiency and gastric cancer and the first report of a patient diagnosed with isolated adrenocorticotropic hormone deficiency during the course of chemotherapy for a solid malignant neoplasm. Although the symptoms and signs described in the present report are common observations during chemotherapy, it is important to consider not only the adverse effects of antineoplastic agents, but also isolated adrenocorticotropic hormone deficiency as a differential diagnosis. Hydrocortisone replacement therapy for isolated adrenocorticotropic hormone deficiency effectively avoids the unnecessary cessation of chemotherapy.

【 授权许可】

   
2014 Kinoshita et al.; licensee BioMed Central Ltd.

【 预 览 】
附件列表
Files Size Format View
20140712103713532.pdf 655KB PDF download
Figure 2. 38KB Image download
Figure 1. 62KB Image download
【 图 表 】

Figure 1.

Figure 2.

【 参考文献 】
  • [1]Steinberg A, Shechter FR, Segal HI: True pituitary Addison’s disease, a pituitary unitropic deficiency; fifteen-year follow-up. J Clin Endocrinol Metab 1954, 14:1519-1529.
  • [2]Yamamoto T, Kamoi K: Prevalence of maturity-onset isolated ACTH deficiency (IAD) in 2005: Japanese cohort studies. Endocr J 2008, 55:939-941.
  • [3]Yamaguchi H, Nakamura H, Mamiya Y, Yamamoto Y, Tajika K, Sugihara H, Gomi S, Inokuchi K, Hasegawa S, Shibazaki T, Dan K, Wakabayashi I: Acute lymphoblastic leukemia with isolated adrenocorticotropic hormone deficiency. Intern Med 1997, 36:819-821.
  • [4]Kamiya Y, Murakami M: Type 2 diabetes mellitus accompanied by isolated adrenocorticotropic hormone deficiency and gastric cancer. Intern Med 2009, 48:1031-1035.
  • [5]Miyauchi S, Yamashita Y, Matsuura B, Onji M: Isolated ACTH deficiency with Graves’ disease: a case report. Endocr J 2004, 51:115-119.
  • [6]Kalambokis G, Vassiliou V, Vergos T, Christou L, Tsatsoulis A, Tsianos EV: Isolated ACTH deficiency associated with Crohn’s disease. J Endorinol Invest 2004, 27:961-964.
  • [7]Gürlek A, Nar A, Gedik O: Isolated adrenocorticotropic hormone deficiency, thyroid autoimmunity, and transient hyperprolactinemia. Endocr Pract 2001, 7:102-105.
  • [8]Corcuff JB, Lafranque P, Henry P, Roger P: Isolated corticotroph insufficiency associated to myasthenia gravis. J Endocrinol Invest 1997, 20:669-671.
  • [9]Sakane N, Yoshida T, Yoshioka K, Umekawa T, Kondo M: Severe hypoglycemia and type I diabetes with isolated ACTH deficiency. Diabetes Care 1995, 18:1621-1622.
  • [10]Sugiura M, Hashimoto A, Shizawa M, Tsukada M, Maruyama S, Ishido T, Kasahara T, Hirata T: Heterogeneity of anterior pituitary cell antibodies detected in insulin-dependent diabetes mellitus and adrenocorticotropic hormone deficiency. Diabetes Res 1986, 3:111-114.
  • [11]de Luis DA, Aller R, Romero E: Isolated ACTH deficiency. Horm Res 2008, 49:247-249.
  • [12]Burke CW: Adrenocortical insufficiency. Clin Endocrinol Metab 1985, 14:947-976.
  • [13]Hannon MJ, O’Halloran DJ: Isolated acquired ACTH deficiency and primary hypothyroidism: a short series and review. Pituitary 2011, 14:358-361.
  • [14]Levinsky NG: Fluids and electrolytes. In Harrison’s Principles of Internal Medicine. 13th edition. Edited by Isselbacher KJ, Braunward E, Wilson JD, Martin JB, Fauci AS, Kasper DL. St Louis: McGraw-Hill; 1994:246.
  文献评价指标  
  下载次数:18次 浏览次数:8次