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Ectopic Cushing's syndrome: experience from a tertiary care centre.

Background & objectives: Ectopic secretion of adrenocorticotropic hormone (ACTH) is rare, contributing to 10 per cent cases of endogenous Cushing's syndrome. We describe our experience of about two decades of patients with ectopic Cushing's syndrome (ECS) seen at a tertiary care centre from north India.

Methods: Records of patients with ECS from 1985 to 2006 were retrospectively reviewed that included the presenting manifestations, clinical symptoms and signs, biochemical investigations including plasma cortisol, ACTH and high dose dexamethasone suppression test (HDDST), imaging modalities to localize the non pituitary source of ACTH production, management and follow up of these patients.

Results: The study group included 12 patients (7 men) with mean ([+ or -] SD) age at presentation 27.6 [+ or -] 9.5 yr (range 13 to 48 yr) and the mean lag period between onset of symptoms and the diagnosis was 18.3 [+ or -] 12.9 months with a range of 3 to 48 months. The weight loss (41.7%) followed by hyperpigmentation (25%) and infections (16.7%) were the common presenting manifestations. Cuticular atrophy (100%), hypertension (100%), bruise (92%) and proximal myopathy (83%) were the commonest signs. Plasma cortisol at 0800 h was 1267.3 [+ or -] 483.3 nmol/l and at 2200 h was 1214.9 [+ or -] 442.6 nmol/l indicating loss of circadian rhythm. The mean plasma ACTH was 221.1 [+ or -] 55.9 (range 21.7 to 950 pg/ml). All but 2 patients had non-suppressibility of 0800 h plasma cortisol with HDDST. Five patients had thymic earcinoid, 3 had bronchial and one each had islet, hepatic and gut carcinoid and one had medullary thyroid carcinoma as a cause of ectopic ACTH secretion. The mean duration of follow up of these patients was 42.6 months and only two could sustain cure while remaining had either residual or recurrence.

Interpretation & conclusion: Ectopic Cushing's syndrome is a rare disease with varied manifestations and associated with increased morbidity and mortality. It presents with clinical features quite similar to classical Cushing's. Surgery with removal of primary tumour was found to be treatment of choice.

Key words Carcinoid--corticotrophin--Cushing's disease--ectopic Cushing's syndrome--neuroendocrine tumour

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Cushing's syndrome refers to the symptoms and signs that result from excessive tissue exposure to glucocorticoids. Endogenous Cushing's syndrome is inordinately (75-80%) caused by adrenocorticotropic hormone (ACTH) secreting pituitary adenomas and the remaining 20-25 per cent is contributed by adrenal neoplasias (10-15%) and ectopic ACTH secretion (10%) (1,2). Non pituitary (ectopic) sources of ACTH include small cell carcinoma of the lung in half the patients and rest are from the various neuroendocrine tumours namely bronchial and thymic carcinoids, and rarely from gut carcinoid (3,4). Ectopic Cushing is very rare with a prevalence of one case per million per year and most of these have been described as lone case reports and a few series (3-17).

Characteristically ectopic ACTH production is said to cause a clinical syndrome which, unlike pituitary dependent Cushing disease is of rapid onset associated with rapid weight loss, muscle weakness, hypokalemic metabolic alkalosis, glucose intolerance, high levels of plasma cortisol and ACTH. In such patients there is usually an obvious underlying tumour and most commonly it is a small cell carcinoma of the lung. However, relatively benign tumours, in particular slowly growing carcinoid tumours (2,3) can give rise to a clinical syndrome which is indistinguishable from pituitary Cushing disease. Clinical manifestations of glucocorticoid and/or androgen excess may be the only clues for carcinoids, though they sometimes may present with marked hyperpigmentation, diarrhoea, flushing, and/or palpitations (18). Biochemically, these neoplasms have been described to secrete various biologically active substances including gastrin, insulin, calcitonin and vasoactive intestinal peptide, as well as corticotropin. Nevertheless, localization of ectopic source of ACTH is not always easy and sometimes it could be delayed from months to years. Because of this, these patients have increased morbidity and consequently culminating into enhanced mortality. We describe our experience of patients with ectopic Cushing's syndrome from a tertiary care centre in north India, seen during last 22 years.

Material & Methods

Between 1985 and 2006, 156 patients attending Endocrine Clinic at Nehru Hospital, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, were diagnosed to have endogenous Cushing's syndrome (CS). Of these 12 had ectopic ACTH syndrome constituting 7.7 per cent of cases. The case records of these patients were reviewed retrospectively. The diagnosis of Cushing's syndrome was based on clinical features of protein catabolism and/or features of androgen excess. Protein catabolism was evident in the form of striae, easy bruisability, muscle weakness, and cuticular and pulp atrophy. Androgen excess manifested as hirsutism, virilization and defeminization as oligo/amenorrhoea in women. The diagnosis of endogenous Cushing's syndrome was based on stepwise approach: first, the definitive determination of the presence of hypercortisolemic state; second whether CS is ACTH dependent or not, and third if CS is ACTH dependent, then localization of the source of ACTH production. Biochemically, diagnosis was based on elevated basal cortisol levels with loss of circadian rhythm, inappropriately elevated ACTH levels in relation with 2200 h cortisol and nonsuppressible serum cortisol to low dose dexamethasone. ACTH dependency of CS was indicated by high ACTH levels (> 23 pg/ml) in the presence of elevated cortisol levels (>210 nmol/l) (26).

The ectopic source of ACTH was localized by imaging including computerized tomography, (Light speed GE Medical System, USA) and magnetic resonance imaging (Somatom, Siemens, Germany 1.5 Tesela) wherever indicated in all of these patients.

Biochemical methods: Plasma cortisol was measured by in-house radioimmunoassay (RIA) by using tritium labelled cortisol after dextran charcoal separation with intra-assay and inter-assay coefficients of variation being <8 per cent (19). Plasma ACTH was measured by immunoradiometric assay (Immulite, 2500 ACTH, Germany). Low dose dexamethasone suppression test (LDDST) followed by high dose dexamethasone suppression test (HDDST) were performed as per Liddle's protocol (20). Loss of circadian rhythm was defined as cortisol levels at 2200 h being more than 50 per cent of the 0800 h values. Suppression of 0800 h plasma cortisol to <140 nmol/l after LDDST and failure to suppress 0800 h cortisol by 50 per cent of basal 0800 h value following HDDST was considered as nonsuppressible. Oral glucose tolerance test with 75 g glucose and measurement of serum electrolytes were performed in all the patients.

Results

Twelve patients were diagnosed to have ectopic Cushing's syndrome (ECS) including 7 men and 5 women. Their age ranged between 13 to 48 yr with mean [+ or -] SD of 27.6 [+ or -] 9.5 yr. The mean ([+ or -] SD) lag period between onset of symptoms and diagnosis was 18.3 [+ or -] 12.9 months with a range of 3 to 48 months.

The presenting manifestations, and symptoms and signs are summarized in Tables I. They had mean ([+ or -] SD) body mass index (BMI) of 22.9 [+ or -] 3.7 kg/[m.sup.2]. Eight (66.7%) patients presented with weight gain and four (33.3%) with weight loss. The clinical presentation was quite typical in 7 patients and unusual in 5 patients. Among unusual manifestations, two patients presented with manic depressive psychosis, one patient each sought medical advice for dry cough, recurrent loose motions, and recurrent pyoderma. The clinical signs included, hypertension and cuticular atrophy in all (100%), bruises in 11 (92%), proximal muscle weakness in l0 (83.3%), hyperpigmentation in 9 (75%), centripetal obesity in 7 (58.3%), and striae in 8 (66.7%). Two boys did not have signs of puberty, while 4 of 5 (80%) of women were oligo/amenorrhoeic. One had vertebral collapse at presentation.

On biochemical evaluation, 7 (58.3%) patients were found to be diabetic while hypokalemia (< 3.5 mEq/l) with metabolic alkalosis was present in 5 (41.7%). All patients failed to demonstrate the normal circadian rhythm of plasma cortisol (Table II), and had inappropriately elevated levels of ACTH at 2200h (where measured) in relation with cortisol. The mean plasma cortisol at 0800 h was 1267.3 [+ or -] 483.3 nmol/l with a range of 600-2400 nmol/l, and at 2200 h was 1214. 9 [+ or -] 442.6 nmol/l with a range of 480-2000 nmol/l. The mean plasma ACTH was 221.1 [+ or -] 55.9 pg/ml. The mean plasma cortisol after LDDST was 1140.75 [+ or -] 434.1 nmol/l showing nonsuppressibility in all the 12 patients. The mean plasma cortisol after HDDST was 943.6 [+ or -] 385.3 nmol/l and depicting nonsuppressibility in l0 (83.3%) out of 12 patients. Urinary hydroxylindoleacetic acid (HIAA) was elevated in 2 (16.7%) patients only.

Tumour localization: Localization of the source of ACTH in these patients, as some of them had unusual sites of carcinoid, was difficult and led to considerable delay. Ultrasonography of the abdomen revealed tumour of the pancreas in one patient as he presented with palpable mass in the epigastrium, and nodular lesions in the liver in another patient. CT scan of the chest localized anterior mediastinal mass in five patients. The bronchial masses were located in right upper lobe and middle lobe in one patient each (Fig. 1a) and a nodule in the left bronchus was found in one patient. Other methods of localization included colonoscopy in one patient who underwent the same for recurrent diarrhoea and was found to have colonic polyps (Table II). The patient who had thyroid nodule on palpation, FNAC confirmed the diagnosis of medullary thyroid carcinoma (MTC). Bilateral adrenal hyperplasia (Fig. 1b) was present in 9 patients and remaining three had normal adrenals. MRI/CT of the pituitary was performed in 10 and only one showed diffuse enlargement, which regressed after curative surgery for bronchial carcinoid (Fig. 1c, 1d). All patients except one who presented with thyroid nodule, showed carcinoid picture on histopathology with nesting trabecular pattern of round cells with rosette formation with fibrovascular core. Cytoplasm was amphophilic with prominent nuclear chromatin (Fig. 2) suggestive of carcinoid. ACTH immunostaining on respective tumour tissues was positive in all four patients, in whom it was available (Fig. 2).

Management and outcome: Of the five patients with thymic carcinoids, three patients underwent surgery with excision of the tumour. In these three patients the surgery was successful, and they were cured of the disease clinically as well as biochemically postoperatively. But they all had recurrence during follow up at variable period of 30-84 months and all three died, two because of metastatic disease, the third one died unattended at home. One patient had anterior mediastinal widening with Hounsefeld value of -40 on CT chest suggestive of lipomatosis (Fig. 3a). He had normal pituitary on MR imaging and underwent bilateral adrenalectomy. During follow up, 6 months later, he presented with rapidly increasing diffuse hyperpigmentation and repeat CT chest showed anterior mediastinal mass invading surrounding large vessels (Fig. 3b), which on aspiration cytology proved to be thymic carcinoid. He received chemotherapy and radiotherapy as primary was inoperable. One patient with thymic carcinoid refused for surgery.

[FIGURE 1 OMITTED]

All three patients with the bronchial carcinoids underwent surgery with removal of the tumour. In one patient, it was successful, other had recurrence with no localization thereafter, and required bilateral adrenalectomy, and the third patient died of acute respiratory distress syndrome post-operatively. Patient with islet cell carcinoid was subjected to bilateral adrenalectomy and also received chemotherapy as the primary was inoperable. Patient with medullary thyroid carcinoma had liver metastasis. She underwent total thyroidectomy along with bilateral adrenalectomy, following which she received chemotherapy. Bilateral adrenalectomy was performed in patient with apparent 'primary' hepatic carcinoid followed by chemotherapy, somatostatin long acting repository (LAR) and metaiodobenzyl guanidine (MIBG) therapy. Even after extensive search and exploratory laparotomy primary lesion could not be found elsewhere therefore it was more likely to be 'primary' hepatic carcinoid. Polypectomy was curative in patient with gut carcinoid, but she also had recurrence and is on ketoconazole therapy. Mean ([+ or -] SD) duration of follow up was 42.6 [+ or -] 19.8 months with range of 0-84 months. Of the 12 patients, eight died and three continue to be in our follow up, while one patient was lost to follow up (Table II).

[FIGURE 2 OMITTED]

[FIGURE 3 OMITTED]

Discussion

This study presents Cushing's syndrome due to ectopic corticotropin (ACTH) production by the neuroendocrine tumours arising from the various sites. Unlike Cushing's disease, with an 8:1 female to male preponderance, this syndrome is more common in men (2) as shown in our study as well. Earlier it has been reported that ectopic secretion of ACTH is most often from small cell carcinomas of the lung (21). But, later reports (3,9) indicate that bronchial carcinoid tumour is the single most common cause. While Medonca et al. (10) reported most common cause as thymic carcinoid in 3 of 8 (37%) patients, as found in our study as well (Table III), and other well documented cases included medullary thyroid carcinoma (3), pheochromocytoma (3), medullary paraganglioma (11), pancreatic islet cell tumours (3), and tumours of the ovary (22), cervix (22) and prostrate (22). A lone case of ectopic ACTH secretion associated with non neoplastic inflammatory mass and cure after its excision has also been described (12). The Cushing's syndrome due to 'primary' hepatic carcinoid is very rare and has been reported by us earlier (13). We did not observe ECS secondary to small cell carcinoma of the lung probably because of lack of typical Cushingoid features, so these would have been missed by treating physicians and/or rapid downhill course prior to referral to our centre.

Corticotropin (ACTH) secreting carcinoid tumours, usually present with clinical features indistinguishable from pituitary dependent Cushing's syndrome (2). This clinical situation is frequently referred to as 'occult' ectopic ACTH syndrome. The reason behind this might be the indolent course of carcinoids and as reported in 44 per cent of patients, the neoplasm was initially occult (3). Therefore, the clinical course is often prolonged and the delay to ultimate diagnosis varying up to 15 yr (3-13) as also shown in our study with a mean lag time of 18 months.

Most reliable signs of Cushing's syndrome include the presence of proximal myopathy, easy bruising and thinness and fragility of skin. At least one of these signs was present in all of these patients. Cuticular atrophy as a sign was present in all of patients, and has been under-reported in other series (3). Prevalence of proximal muscle weakness, diabetes mellitus was similar to other series (3), while bruising, striae and weight loss were more common in our patients as compared to other studies (3). Another clue to diagnosis of ectopic ACTH secretion from carcinoids are clinical manifestations due to simultaneous secretion of other metabolically active substances. Two of the patients had diarrhoea at presentation which may indicate secretion of vasoactive intestinal peptide (VIP) from the carcinoid tumours. Lack of age appropriate pubertal signs in two boys can be explained on the basis of direct suppressive effect of cortisol on pituitary gonadotropes and testis as well. Biochemically, ectopic ACTH syndrome is frequently associated with exceedingly high circulating concentrations of corticotropin (23), as seen in our patients. The presence of hypokalemia is another biochemical clue that glucocorticoid excess is mediated by ectopic production of corticotropin (24). The apparent reason for the hypokalemia is the saturation of 11-[beta]-hydroxysteroid dehydrogenase type 1 by excessive cortisol, which under normal circumstances protects the mineralocorticoid receptors from the effects of cortisol (25). However this generally reflects the prevailing levels of cortisol rather than the specific aetiology. In our series, 5 of the 12 patients had hypokalemia at presentation.

Liddle and associates (20) reported that administration of dexamethasone in high-dose (16 mg) did not suppress cortisol in 94 per cent of cases of ECS. Consistent with this, 83.3 per cent of our patients had non-suppressibility to high dose dexamethasone. Nevertheless, suppressibility of cortisol after high dose dexamethasone had been shown in slowly growing bronchial carcinoids thereby rendering them difficult to differentiate from pituitary Cushing's disease (26). Carcinoid tumours are often associated with increased levels of urinary 5-hydroxyindoleacetic acid (5-HIAA), a metabolite of serotonin. However, foregut carcinoids, which include bronchial carcinoids as well do not have increased 5-HIAA levels, as was also seen in our study.

Efforts to identify an ectopic source of ACTH secretion is not always successful as happened in one of our patient (8.3%). This result is similar to that of the other study (17). In our study thoracic tumour was the source of ectopic secretion in 66.7 per cent of cases, similar to that reported by others (3). Tumours were best localized with CT thorax/abdomen in > 80 per cent of cases. However, in case of failure to localize the ectopic source of ACTH secretion with one modality, multiple imaging techniques should be employed to identify the same. Thus, as suggested by Ilias et al (3) CT, MRI and octreotide scan/PET scan all may be required to localize the ectopic source of ACTH secretion. In one of our patient mediastinal widening was interpreted as mediastinal lipomatosis and later after bilateral adrenalectomy, he presented with inoperable thymic carcinoid. Other imaging modalities and/or cytology might have helped to localize the lesion initially. In our study CT/MRI

of the sella was normal in all patients, where it was performed, except in one who had pituitary hyperplasia. This might be due to corticotropin releasing hormone (CRH) secretion from the carcinoid, as it regressed after removal of the bronchial carcinoid. However, incidental adenomas of the pituitary gland are present in up to 35 per cent of adults (27), thus that hypophysectomy occasionally yields a nonfunctioning pituitary adenoma in patients with ectopic ACTH syndrome, is not surprising. On the contrary, even in the presence of pituitary adenoma in a patient with Cushing's disease, MRI may not reveal the source in up to 50 per cent of cases. Bilateral inferior petrosal sinus sampling seems to be the most accurate method for distinguishing pituitary from ectopic production of corticotrophin (1). A basal inferior petrosal sinus to peripheral blood (IPS: P) ratio of [greater than or equal to] 2 and a peak IPS: P ratio of [greater than or equal to] 3 is suggestive of pituitary as a source of ACTH production. However, this may be misleading in ectopic CRH producing tumours (1). Immunostaining positivity for ACTH on tumour tissue strongly supports the tissue source of its ectopic production.

Surgery is often curative for both the neoplasm and the associated glucocorticoid excess as was performed in 66.7 per cent of cases similar to that of 65 per cent reported by others (3). The role of adjuvant radiotherapy, chemotherapy, or both have not been accurately assessed because of the lesser number of cases (1). Nevertheless, post-operative radiotherapy may be helpful in preventing local recurrence after excision of an invasive carcinoma (1,3). Bilateral adrenalectomy was required in one third of patients either because inoperable primary or because of recurrence. This figure is similar to that reported by Ilias et al (3). Of the twelve patients, three continue to be in our follow up with a mortality of 66.7 per cent during mean follow up duration of 42.6 months which is higher than what has been reported earlier (18% in 26 months follow up) (3). This possibly is related to delayed presentation, and irregular follow up.

In conclusion, ectopic ACTH syndrome due to slowly growing tumours like carcinoids usually presents with clinical features indistinguishable from classical Cushing's. Primary tumour in majority of instances could be localized with CT scan. Single imaging can give false positive results. Surgery with removal of primary tumour is the treatment of choice and is often curative but needs regular surveillance for recurrence.

Received June 8, 2007

References

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(2.) Linsay JR, Nieman LK. Differential diagnosis and imaging in Cushing syndrome. Endocrinol Metab Clin North Am 2005; 34 : 403-21.

(3.) Ilias L, Torpy DJ, Pacak K, Mullen N, Wesley RA, Nieman LK. Cushing's syndrome due to ectopic ACTH secretion. Twenty years' experience at National Institute of Health. J Clin Endocrinol Metab 2005; 90 : 4955-62.

(4.) Azzopardi JG, Williams ED. Pathology of "non endocrine tumours" associated with Cushing's syndrome. Cancer 1968; 22 : 274-86.

(5.) Wang DY, Chang DB, Kuo SH, Yang PC, Lee YC, Hru HC, et al. Carcinoid tumours of the thymus. Thorax 1994; 49: 357-60.

(6.) Teh BT, Zedenius J, Kytola S, Skogseid B, Trotter J, Choplis H, et al. Thymic carcinoids in multiple endocrine neoplasm type 1. Ann Surg 1998; 228 : 99-105.

(7.) Clark ES, Carney JA. Pancreatic islet-cell tumour associated with Cushing's syndrome. Am J Surg Pathol 1984; 8 : 917-24.

(8.) Findling JW, Turrell JB. Occult ectopic secretion of corticotropin. Arch Intern Med 1986; 146 : 929-33.

(9.) Saeger W, Reincke M, Schoz GH, Ludecke DK. Ectopic ACTH-or CRH-secreting turnours in Cushing's syndrome. Zentralbl Pathol 1993; 139 : 157-63.

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(11.) Schteingast DE, Conn JW, Orth DN, Harrison TS, Fox JE, Book Stein JJ, et al. Secretion of ACTH and MSH by an adrenal medullary paraganglioma. J Clin Endocrinol 1972; 34 : 676-83.

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(14.) Velayntham P, Bhansali A, Shfiram M, Thingnam S, Mather S. A young man with weight loss and depression. Postgrad Med J 2004; 80 : 243-6.

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(16.) Gupta V, Banerjee CK, Singh H, Suri S, Dash R.J. Thymic carcinoid with ectopic Cushing's syndrome. J Assoc Physicians India 1990; 38 : 862-84.

(17.) Aniszewski JP, Young WFJ, Thompson GB, Grant CS, Van Heerden JA. Cushing syndrome due to ectopic adrenocorticotropic hormone secretion. World J Surg 2001; 25 : 934-40.

(18.) Oberg K. Carcinoid tumours, carcinoid syndrome, and related disorders. In: Larsen PR, Kronenberg HM, Melmed S, Polonsky KS, editors. Williams textbook of endocrinology. Philadelphia: Saunders; 2002. p. 1852-76.

(19.) Dash RJ, England BG, Midgley AR Jr, Niswender G. A specific, non chromatographic radio immunoassay for human plasma cortisol. Steroids 1975; 26 : 647-61.

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(21.) Liddle GW, Island DP, Ney RL, Nicholson WE, Shimizu N. Nonpituitary neoplasm and Cushing syndrome. Ectopic "adrenocorticotropin" produced by nonpituitary neoplasm as a cause of Cushing's syndrome. Arch Intern Med 1963; 111 : 471-5.

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(24.) Howler TA, Drury PL, Perry L, Doniach I, Rees LH, Besser GM. Diagnosis and management of ACTH-dependent Cushing's syndrome: comparison of the features in ectopic and pituitary ACTH production. Clin Endocrinol (Oxf) 1986; 24 : 699-713.

(25.) Stewart PM, Walker BR, Holder G, O'Halloran D, Shackleton CH. 11 Beta-hydroxysteroid dehydrogenase activity in Cushing's syndrome: explaining the mineralo corticoid excess state of the ectopic adrenocorticotropin syndrome. J Clin Endocrinol Metab 1995; 80 : 3617-20.

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Reprint requests: Dr Anil Bhansali, Department of Endocrinology, Postgraduate Institute of Medical Education & Research Chandigarh 160 012, India

e-mail: anilbhansali_endocrine@rediffmail.com

A. Bhansali, Rama Walia, S.S. Rana *, P. Dutta, B.D. Radotra **, N. Khandelwal ([dagger]) & S.K. Bhadada

Departments of Endocrinology, * Cardiothoracic Surgery, ** Pathology & ([dagger]) Radiodiagnosis, Postgraduate Institute of Medical Education & Research, Chandigarh, India
Table I. Presenting manifestation and signs and symptoms
in patients with ectopic Cushing's syndrome (n = 12)

Presenting manifestations No. (%)

Weight loss 4 (33.3)
Hyperpigmentation 2 (25)
Recurrent loose motions 2 (16.7)
Infections Recurrent
 pyoderma (1), Pneumonia (1) 2 (16.7)
Dry cough 1 (8.3)
Manic depressive psychosis 1 (8.3)

Signs & symptoms No. (%)

Cuticular atrophy 12 (100)
Hypertension 12 (100)
Bruise 11 (91.7)

Proximal myopathy 10 (83.3)
Hyperpigmentation 9 (75)
Centripetal obesity 8 (66.7)
Strige 8 (66.7)
Diabetes 7 (58.3)
Menstrual irregularities 4/5 (80)
Hirsutism 1/5 (20)

Table II. Profile of patients with
ectopic Cushing's syndrome

Sr. Age/ Lag time Cortisol LDD HDD ACTH
No. sex in (nmol/l) pg/ml
 months
 AM PM

1 34 M 18 1480 1500 1400 1200 359
2 31 M 12 1400 1680 1360 1280 950
3 32 F 24 1200 1100 640 640 96
4 32 M 3 600 480 160 1200 100
5 30 M 36 900 900 840 370 72
6 22 F 6 600 640 440 660 22
7 19 M 48 1380 1560 1080 370 88
8 13 M 12 1048 879 709 703 --
9 22 M 12 1600 1280 1260 1240 --
10 47 F 24 2400 2000 2000 1500 --
11 33 F 12 1400 1200 1200 900 191
12 16 F 12 1200 1360 1200 1260 112

Sr. Primary Method of Management
No. site / H/P localization

1 Thymic carcinoid CT chest Surgery
2 Thymic carcinoid CT chest Surgery + RT
3 Thymic carcinoid CT chest Surgery
4 Thymic carcinoid CT chest Lost to F/U
5 Thymic carcinoid CT chest B/L adrenalectomy
6 Bronchial carcinoiod CT chest Surgery
7 Bronchial carcinoiod CT chest Surgery
8 Bronchial carcinoiod CT chest Surgery
9 Islet carcinoid USG abdomen B/L adrenalectomy+CT
10 Medullary thyroid FNAC Thyroid surgery+
 carcinoma B/L adrenalectomy
11 Liver carcinoid CT abdomen B/L adrenalectomy+CT
12 Colonic carcinoid Colonoscopy Surgery

Sr. Outcome Present Follow up
No. status (months)

1 Recurrence-RT Died 30
2 Recurrence-RT Died 42
 and CT

3 Recurrence Died 84
4 -- -- --
5 Overt Died 36
 [arrow right]
 CT + RT

6 Cure Surviving 42

7 Recurrence Surviving 54
 [arrow right]
 B/L adrenalectomy
 CT,RT
 [arrow right]
 cure

8 Post-op ARDS Died --
9 Residual Died 6
10 Rccurrencc Died 48
11 Residual Died 36
12 Reccurrence Surviving 48

CT, chemotherapy; RT, radiotherapy; F/U, Follow up,
B/L, bilateral; LDD, low dose dexamethasone:
HDD, high dose desamethasone; FNAC, five needle
aspiration cytology; USG, ultrasonography;
ARDS, adult respiratory distress syndrome

Table III. Causes of the ectopic ACTH syndrome

 Ilias Saeger Mendonca
 et et et Present
 al (3) al (9) al (10) study

N 90 13 8 12
Thymic carcinoid 5 1 3 5
Bronchial carcinoid 35 4 1 3
Appendiceal carcinoid 1 -- -- --
Neuroendocrine tumour 13 -- -- --
Pulmonary tumourlets 1 -- -- --
Gastroinoma 6 -- -- --
Small cell lung cancer 3 1 -- --
Pheochromocytoma 5 1 1 --
Medullary thyroid 2 2 1 1
 carcinoma
Islet carcinoid 1 2 2 1
Pancreatic carcinoid 1 2 2 0
Prostatic cancer -- 1 -- --
Liver carcinoid -- -- -- 1
Colonic carcinoid -- -- -- 1
Miscellaneous 1 1 -- --
Unknown/occult 17 -- -- --
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Author:Bhansali, A.; Walia, Rama; Rana, S.S.; Dutta, P.; Radotra, B.D.; Khandelwal, N.; Bhadada, S.K.
Publication:Indian Journal of Medical Research
Article Type:Report
Geographic Code:9INDI
Date:Jan 1, 2009
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