scholarly journals A Severe Hypokalemia Case Due to Ectopic Acth Syndrome Secondary to Small Cell Lung Cancer

2018 ◽  
Vol 3 (4) ◽  
pp. 145-148
Author(s):  
Edip Erkus ◽  
◽  
M. Zahid Kocak ◽  
Gulali Aktas ◽  
Emine Ozsari ◽  
...  
Haigan ◽  
2012 ◽  
Vol 52 (4) ◽  
pp. 387-392
Author(s):  
Kiyoharu Fukushima ◽  
Yoshiyuki Saito ◽  
Takeshi Uenami ◽  
Naotoshi Tsuruta ◽  
Takashi Niju ◽  
...  

2003 ◽  
Vol 26 (2) ◽  
pp. 187
Author(s):  
Hyun-Ju Song ◽  
Kum-Hei Ryu ◽  
Su-Hyun Kim ◽  
Su-Jin Yoon ◽  
Do-Yeun Kim ◽  
...  

Author(s):  
Hiroki Nakajima ◽  
Yasuhiro Niida ◽  
Eriko Hamada ◽  
Kuwata Hirohito ◽  
Masahide Ota ◽  
...  

Summary Ectopic ACTH (adrenocorticotrophic hormone) syndrome (EAS) is rarely associated with small-cell lung cancer (SCLC). Although chemotherapy is initially effective for SCLC, complicated EAS scarcely improves. Recently, immune checkpoint inhibitors have been used to treat SCLC. Atezolizumab plus chemotherapy for SCLC improved progression-free survival compared to conventional chemotherapy. However, little has been reported on the efficacy of the combination therapy for SCLC with EAS. We report a 72-year-old male who presented with 4-week history of leg oedema, proximal myopathy, weight loss, and worsened symptoms of diabetes and hypertension. Laboratory findings revealed hypokalaemia, increased plasma ACTH, and serum cortisol levels. Cortisol levels were not suppressed by the high-dose dexamethasone test. Chest and abdominal CT revealed a right lower lobe tumour with multiple metastases on the hilar lymph nodes, liver, lumbar spine, and bilateral enlarged adrenal glands. The patient was diagnosed with stage 4B SCLC with EAS. Hypercortisolaemia was then treated with metyrapone and atezolizumab plus chemotherapy, which was started for SCLC. After 10 days, the tumour shrank noticeably, and the ACTH level drastically decreased concomitantly with low cortisol levels with symptoms of fever, appetite loss, and general fatigue. Hydrocortisone treatment was initiated, and the symptoms resolved immediately. We describe a case of SCLC with EAS treated with atezolizumab plus chemotherapy, presenting with adrenal insufficiency. Close observation is required for patients with adrenal insufficiency receiving atezolizumab plus chemotherapy because of its stronger effect. Furthermore, advances in cancer therapy and care for endocrine paraneoplastic syndrome needs to be adapted. Learning points The immune checkpoint inhibitor atezolizumab has recently been approved for the treatment of small-cell lung cancer (SCLC). Approximately 1–6% of tumour ectopically produce ACTH and cause ectopic ACTH syndrome (EAS) as an endocrine paraneoplastic syndrome. The use of combined chemotherapy and atezolizumab in the ectopic ACTH syndrome secondary to small-cell lung cancer may cause a precipitous fall in circulating ACTH/cortisol, resulting in symptomatic adrenal insufficiency The advances in cancer therapy and treatment for endocrine paraneoplastic syndrome need to be adapted.


Onkologie ◽  
2009 ◽  
Vol 32 (7) ◽  
pp. 11-11 ◽  
Author(s):  
Chin-Jung Lin ◽  
Wann-Cherng Perng ◽  
Chien-Wen Chen ◽  
Chih-Kung Lin ◽  
Wen-Lin Su ◽  
...  

2007 ◽  
Vol 22 (5) ◽  
pp. 359 ◽  
Author(s):  
Hong Jun Yang ◽  
Hea Jung Sung ◽  
Ji Eun Kim ◽  
Hyo Jin Lee ◽  
Jin Min Park ◽  
...  

2011 ◽  
Vol 2011 (aug04 1) ◽  
pp. bcr0420102917-bcr0420102917 ◽  
Author(s):  
S. I. Aziz ◽  
M. A. Khattak ◽  
Z. Usmani ◽  
N. Ladipeerla ◽  
K. Pittman

2010 ◽  
Vol 17 (1) ◽  
pp. 203-213 ◽  
Author(s):  
Paula Sommer ◽  
Rachel L Cowen ◽  
Andrew Berry ◽  
Ann Cookson ◽  
Brian A Telfer ◽  
...  

Small cell lung cancer (SCLC) is an aggressive tumor, associated with ectopic ACTH syndrome. We have shown that SCLC cells are glucocorticoid receptor (GR) deficient, and that restoration of GR expression confers glucocorticoid sensitivity and induces apoptosis in vitro. To determine the effects of GR expression in vivo, we characterized a mouse SCLC xenograft model that secretes ACTH precursor peptides, and so drives high circulating corticosterone concentrations (analogous to the ectopic ACTH syndrome). Infection of SCLC xenografts with GR-expressing adenovirus significantly slowed tumor growth compared with control virus infection. Time to fourfold initial tumor volume increased from a median of 9 days to 16 days (P=0.05; n=7 per group). Post-mortem analysis of GR-expressing tumors revealed a threefold increase in apoptotic (TUNEL positive) cells (P<0.01). Infection with the GR-expressing adenovirus caused a significant reduction in Bcl-2 and Bcl-xL transcripts. Furthermore, in both the GR-expressing adenovirus-infected cells and tumors, a significant number of uninfected cells underwent apoptosis, supporting a bystander cell killing effect. Therefore, GR expression is pro-apoptotic for human SCLCs in vivo, as well as in vitro, suggesting that loss of GR confers a survival advantage to SCLCs.


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