Abstract:Summary Secretion of ectopic adrenocorticotropic hormone (ACTH) with consequently Cushing's syndrome is a rare paraneoplastic phenomenon. It has been described in a variety of malignancies, like bronchial carcinoids, small-cell lung carcinoma, thymoma, pancreatic carcinoma and other. In many cases of suspected ectopic ACTH secretion, it is difficult to histologically or cytochemically confirm the diagnosis. We present a 63-year-old woman with a recurrent poorly differentiated squamous cell lung carcinoma with … Show more
“…In the recent literature, the incidence of SCLC associated with paraneoplastic syndrome has seemed to decrease (2). A possible explanation for this trend might be the recent improvements in diagnosis, chemotherapy, and radiotherapy.…”
Paraneoplastic Cushing's syndrome caused by ectopic adrenocorticotropin (ACTH) production has been reported. However, most cases of this syndrome are diagnosed before first-line chemotherapy or at the time of disease recurrence. Here, we present a 53-year-old man who gradually developed the symptoms of Cushing's syndrome during effective chemotherapy for small cell lung cancer. His symptoms were controlled using mitotane, but his primary cancer progressed and he died 5 months after the start of chemotherapy. This very rare case of Cushing's syndrome associated with small cell lung cancer during effective chemotherapy is presented here.
“…In the recent literature, the incidence of SCLC associated with paraneoplastic syndrome has seemed to decrease (2). A possible explanation for this trend might be the recent improvements in diagnosis, chemotherapy, and radiotherapy.…”
Paraneoplastic Cushing's syndrome caused by ectopic adrenocorticotropin (ACTH) production has been reported. However, most cases of this syndrome are diagnosed before first-line chemotherapy or at the time of disease recurrence. Here, we present a 53-year-old man who gradually developed the symptoms of Cushing's syndrome during effective chemotherapy for small cell lung cancer. His symptoms were controlled using mitotane, but his primary cancer progressed and he died 5 months after the start of chemotherapy. This very rare case of Cushing's syndrome associated with small cell lung cancer during effective chemotherapy is presented here.
“…Ectopic ACTH secretion has been described in a wide number of neoplasms: non-small-cell lung carcinoma [9], small-cell lung carcinoma, carcinoid tumors (bronchopulmonary, thymic and gastrointestinal origin), pancreatic islet tumors, pheocromocytoma, thyroid's medullary carcinoma [18] and a host of other tumors, such as paraganglioma [19], prostate [20], breast [21,22], kidneys [23], stomach [24], ovaries [25], melanoma [26], colon [27], leukemia [28], anorectal tumors [29], and even in inflammatory tissues [30]. Among these, the bronchopulmonary carcinoid tumor remains the most prevalent [18].…”
Section: Discussionmentioning
confidence: 99%
“…Ten per cent of CS cases are secondary to non-pituitary neoplasms, such as the bronchopulmonary carcinoid tumors and, occasionally, non-small-cell lung tumor [9]. In both cases there is production of excessive amounts of ectopic ACTH.…”
“…Harvey Cushing (1869–1939) described in 1912 an endocrine syndrome caused by pituitary overproduction of adrenocorticotropic hormone (ACTH) 2. In patients with Cushing’s syndrome (CS), an ectopic secretion of ACTH comprises about 5%–10% of cases, and approximately 50%–60% of these are neuroendocrine lung tumours, such as small-cell lung cancer (SCLC) 1 3 4.…”
Ectopic adrenocorticotropic hormone (ACTH) secretion represents 5%-10% of cases of Cushing's syndrome (CS), and approximately 50%-60% of these arise from neuroendocrine lung tumours, including small-cell lung cancer (SCLC). We report a 42-year-old man admitted with hypertension, metabolic alkalosis and severe hypokalaemia. On physical examination, centripetal obesity with 'moon face' and 'buffalo's hump' were identified, and wheezing on left lung was heard. A markedly elevated serum cortisol, ACTH and urine free cortisol production supported the diagnosis of CS. Chest CT showed a left hilar mass with metastasis to the liver, adrenal glands and lymph nodes. Bronchoscopy identified bronchial infiltration by SCLC. Treatment with metyrapone and chemotherapy was started. Despite initial improvement, progressive clinical deterioration occurred, culminating in death 1 year after diagnosis. Ectopic ACTH secretion is uncommon but should be suspected in patients with severe hypokalaemia, hypertension and metabolic alkalosis, especially in the context of lung cancer.
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