Case Reports in Endocrinology

Case Reports in Endocrinology / 2016 / Article

Case Report | Open Access

Volume 2016 |Article ID 4852907 | 4 pages |

An Ectopic ACTH Secreting Metastatic Parotid Tumour

Academic Editor: Hidetoshi Ikeda
Received11 Nov 2015
Revised21 Dec 2015
Accepted22 Dec 2015
Published20 Jan 2016


A 60-year old woman presented with features of Cushing’s syndrome (CS) secondary to an ectopic adrenocorticotropic hormone (ACTH) secreting metastatic parotid tumour 3 years after excision of the original tumour. She subsequently developed fatal intestinal perforation and unfortunately died despite best possible medical measures. Ectopic ACTH secretion accounts for 5–10% of all patients presenting with ACTH dependent hypercortisolism; small cell carcinoma of lung (SCLC) and neuroendocrine tumours (NET) account for the majority of such cases. Although there are 4 previous case reports of ectopic ACTH secreting salivary tumours in literature, to our knowledge this is the first published case report in which the CS developed after 3 years of what was deemed as a successful surgical excision of primary salivary tumour. Our patient initially had nonspecific symptoms which may have contributed to a delay in diagnosis. Perforation of sigmoid colon is a recognised though underdiagnosed complication associated with steroid therapy and hypercortisolism. This case demonstrates the challenges faced in diagnosis as well as management of patients with CS apart from the practical difficulties faced while trying to identify source of ectopic ACTH.

1. Background

Cushing’s syndrome (CS) is associated with a constellation of signs and symptoms related to hypercortisolism. Common conditions such as obesity, chronic alcoholism, and depression share clinical and phenotypic features which overlap with those seen in patients with CS; often it results in delayed investigations and management for the patients.

True CS can either be ACTH dependent or ACTH independent [1]. ACTH dependent CS is uncommon with 1-2 cases/million of population/per year reported in the literature, with pituitary adenoma being source of ACTH in two-thirds of such patients [1]. SCLC and pancreatic/thymic/bronchial NETs remain the commonest tumours associated with ectopic ACTH secretion [24]. There are rare reports linking medullary carcinoma of thyroid, phaeochromocytoma, and ovarian and salivary tumours with ectopic ACTH secretion [5, 6]. To our knowledge, there are only 4 previous case reports of ectopic ACTH secretion from a salivary gland carcinoma leading to CS [710]. This is also the first report of an ectopic ACTH-secreting metastatic salivary tumour in which the CS developed after 3 years of complete and what was deemed as a successful surgical excision of primary salivary tumour.

2. Case Presentation

Mrs. XX, a 60-year-old woman was hospitalised with 5-month history of worsening fatigue, leg swelling, and difficulty in walking. Her past medical history included primary hypothyroidism and hypertension. She had been diagnosed with an acinic cell carcinoma of the left parotid gland, which was resected 3 years prior to current admission. She was under follow-up of the surgical team with no obvious evidence of disease recurrence or relapse at the time of presentation.

On examination in medical assessment unit, she had florid features of CS including central obesity, plethoric face, skin thinning, purplish abdominal striae, and proximal muscle weakness. Her blood pressure was elevated with rest of the general physical and systemic examination being unremarkable.

3. Investigations

Her initial investigations results were as shown in Table 1.

InvestigationsResultsReference range

Haemoglobin 125 g/L 115–155
White blood cell count 11.5 × 109/L 4–10.5
Neutrophils 7.5 × 109/L 1.5–7.5
Platelets 318 × 109/L 150–450
Serum sodium 141 mmol/L 135–145
Serum potassium 2.6 mmol/L 3.5–5.5
Serum urea 3.6 mmol/L 2.5–7.8
Serum creatinine 51 μmol/L 50–100
Fasting blood glucose 7 mmol/L

On the basis of clinical suspicion of hypercortisolism, she underwent further tests as shown in Tables 2 and 3.

InvestigationsResultsReference range

Prolactin 429 mU/L <560
Insulin-like growth factor 1 11 nmol/L 12.0–54.0
24-hour urinary cortisol level 4481 nmol<146
ACTH 106 ng/L 7–63

InvestigationProcedureTiming of the testResults

Overnight dexamethasone test (ODST)1 mg dexamethasone given at midnightMeasurement of 9 am cortisol785 nmol/L
Low dose dexamethasone test (LDDST)0.5 mg dexamethasone given every six hours for 48 hoursCortisol measured after last dose of dexamethasone 577 nmol/L

Magnetic Resonance Image of the Pituitary. It showed normal pituitary gland.

Abdomen/Pelvis/Thorax CT. It shows a lytic lesion on the left ischium bone suggestive of a metastatic carcinoma. A collection of gas around the sigmoid colon was noticed which was suggestive of perforated sigmoid diverticulitis.

Histopathology. Biopsy of ischial lesion showed features consistent with a metastatic poorly differentiated acinic cell carcinoma with negative staining for ACTH (Figure 2). However, the previously resected primary parotid tumour of acinic cell carcinoma were stained positively for ACTH.

4. Treatment

Our patient was commenced on metyrapone therapy on day 6 of admission with a gradual uptitration of the dose. The course of her disease was aggressive with subsequent development of intestinal perforation. Interestingly, she had minimal symptoms and signs on clinical examination suggestive of intestinal perforation with this diagnosis being only established based on the radiological investigations.

She later developed sepsis and was managed in intensive care unit. Unfortunately, despite the best possible care her condition continued to deteriorate and she died due to complications related to her ectopic ACTH related CS secondary to a metastatic salivary gland tumour.

5. Discussion

Ectopic ACTH secreting tumours are rare with a reported prevalence of 8–18% of all the patients with CS [11, 12]. The SCLC along with NETs (bronchial, thymic, and pancreatic) remains the commonest ACTH secreting tumours [24]. Our patient presented with CS secondary to an ectopic ACTH producing metastatic parotid tumour. In our literature search, we could only identify 4 previously reported cases of metastatic salivary tumour associated with ectopic ACTH production [58]. In most of the previous case reports, CS was diagnosed either at the time of diagnosis of primary salivary tumour or within months of commencement of treatment (median duration of CS diagnosis 6 months after initial salivary tumour was detected). Our patient is the first case report of an ectopic ACTH secreting salivary tumour presenting with a distant metastasis after over 3 years of being deemed cured of primary tumour (postsurgical excision).

Our patient presented with 5-month history of nonspecific features including weight gain, malaise, and leg swelling. There was a possible delay in her investigations and management due to nonspecific nature of her symptoms. An overlap of such symptoms is not uncommonly seen in obesity, depression, and chronic alcoholism which have a much higher prevalence in clinical practice.

On admission, our patient had florid signs of CS including proximal myopathy and purple striae which are considered relatively specific for CS [13]. The initial screening (24 hour UFC and ODST) tests were suggestive of hypercortisolism. An unsuppressed cortisol level on LDDST further established the biochemical evidence for CS. Elevated ACTH levels pointed towards possibility of a pituitary or ectopic source of ACTH/CRH. The MRI of pituitary gland was reported as normal in our patient. In clinical practice, it is often challenging to distinguish an ectopic ACTH secreting tumour from a pituitary source especially considering that in 40% of CD patients a MRI pituitary may be normal [14]. Inferior petrosal sinus sampling (IPSS) was considered as the next step in investigation although it could not be carried out as our patient was deemed medically unfit to undergo this invasive procedure. Previously, a HDDST was considered to be a useful additional test to distinguish pituitary from an ectopic source of ACTH. In CD, a cortisol suppression of > 50% from the basal level is noticed in only 80% of the patients undergoing HDDST, limiting the diagnostic usefulness of this test [15]. IPSS remains the gold standard to distinguish pituitary from an ectopic source of ACTH [16].

The ectopic ACTH source may not be obvious initially in patients with well-differentiated neuroendocrine tumours as these are generally slow growing and may not be visualised on routine radiological imaging. In 12% of patients, despite extensive investigations, the source of ectopic ACTH may not be identified [17]. Various modalities have been suggested to investigate and identify source of ectopic ACTH secretion including use of Somatostatin scintigraphy [18]. Proopiomelanocortin (POMC) serves as precursor molecule to ACTH and undergoes posttranslational proteolytic processing in corticotrophs. This proteolysis processing is mediated by serine proteinases such as PC1, PC2, and PC3 which are expressed only in the pituitary gland and play a role in POMC cleavage. Ectopic ACTH tumours are characterised by an abnormal circulating ACTH precursor to ACTH ratio as compared to ACTH secreting pituitary adenoma due to a possible aberrant POMC processing [19, 20]. As no single imaging technique is believed to have optimal accuracy for localisation of ectopic ACTH secreting tumour, it is recommended to combine more than one imaging modality such as conventional CT along with somatostatin scintigraphy scan [18].

A whole body CT scan in our patient revealed a lytic lesion on the left ischial bone and patient went on to develop bowel perforation, with minimal features. Exogenous steroid use and CS have been associated with increased risk of intestinal perforation and sepsis [21, 22]. It is not uncommon for the cortisol excess to mask signs associated with intestinal perforation delaying the diagnosis which can potentially prove fatal as in our patient.

The ischial lytic bone lesion on histopathological analysis was confirmed to be a metastasis from the parotid gland tumour although it was stained negatively for ACTH. The immunostaining of preserved original tumour tissue was stained positively with ACTH confirming the diagnosis (Figure 1). Negative ACTH staining in ectopic tumour tissue is believed to be associated with a more aggressive disease course and a worse prognosis [23]. It is postulated that the tumour which has a high secretory rate gets depleted of all intracellular ACTH which results in negative immunostaining on histopathological analysis as may have been the case in our patient.

The further investigations and treatment were limited in our patient because of her rapid clinical deterioration. In retrospective analysis, we acknowledge the fact that there was a relative delay in initiation of metyrapone therapy in her case. Bilateral adrenalectomy should be considered as a life-preserving treatment option in patients presenting with severe ACTH dependent CS uncontrolled with medical therapy or in patients with metastatic ectopic ACTH secreting tumours [24] although our patient was deemed an unsuitable candidate for any surgical intervention.

In summary, our patient presented with a highly aggressive ectopic ACTH secreting metastatic parotid tumour. Earlier suspicion and management of hypercortisolism could have potentially improved her prognosis although it may or may not have altered the eventual outcome.

Learning Points

(i)The signs and symptoms associated with Cushing’s syndrome may be nonspecific which can potentially lead to a delay in diagnosis and management.(ii)The presence of proximal myopathy, easy bruisability, and purple striae should prompt investigations for CS as untreated disease carries high morbidity and mortality.(iii)Distinguishing pituitary from ectopic source of ACTH is challenging especially if there is no obvious adenoma identified on magnetic resonance imaging (MRI) of the pituitary. This is a recognised clinical scenario in up to 40% of the patients with Cushing’s disease (CD).(iv)SCLC and NETs remain the commonest tumours associated with ectopic ACTH secretion although it has been reported in association with salivary gland, medullary carcinoma of thyroid, phaeochromocytoma, and ovarian tumours.(v)Bilateral adrenalectomy should be considered as a life-preserving treatment option in patients presenting with severe ACTH dependent CS uncontrolled with medical therapy or in patients with metastatic ectopic ACTH secreting tumours.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Supplementary Materials

Supplementary figure showing cortisol level fluctuations despite metyrapone therapy.

  1. Supplementary Material


  1. H. E. Turner and J. A. H. Wass, Oxford Handbook of Endocrinology and Diabetes, Oxford University Press, Oxford, UK, 2nd edition, 2009.
  2. T. A. Howlett, P. L. Drury, L. Perry, I. Doniach, L. H. Rees, and G. M. Besser, “Diagnosis and management of ACTH-dependent Cushing's syndrome: comparison of the features in ectopic and pituitary ACTH production,” Clinical Endocrinology, vol. 24, no. 6, pp. 699–713, 1986. View at: Publisher Site | Google Scholar
  3. F. A. Shepherd, J. Laskey, W. K. Evans, P. E. Goss, E. Johonsen, and F. Khamsi, “Cushing's syndrome associated with ectopic corticotropin production and small-cell lung cancer,” Journal of Clinical Oncology, vol. 10, no. 1, pp. 21–27, 1992. View at: Google Scholar
  4. L. R. Salgado, M. C. B. Villares Fragoso, M. Knoepfelmacher et al., “Ectopic ACTH syndrome: our experience with 25 cases,” European Journal of Endocrinology, vol. 155, no. 5, pp. 725–733, 2006. View at: Publisher Site | Google Scholar
  5. R. C. Smallridge, K. Bourne, B. W. Pearson, J. A. Van Heerden, P. C. Carpenter, and W. F. Young, “Cushing's syndrome due to medullary thyroid carcinoma: diagnosis by proopiomelanocortin messenger ribonucleic acid in situ hybridization,” Journal of Clinical Endocrinology and Metabolism, vol. 88, no. 10, pp. 4565–4568, 2003. View at: Publisher Site | Google Scholar
  6. E. H. Al Ojaimi, “Cushing's syndrome due to an ACTH-producing primary ovarian carcinoma,” Hormones, vol. 13, no. 1, pp. 140–145, 2014. View at: Google Scholar
  7. M. Sugawara and G. A. Hagen, “Ectopic ACTH syndrome due to salivary gland adenoid cystic carcinoma,” Archives of Internal Medicine, vol. 137, no. 1, pp. 102–105, 1977. View at: Publisher Site | Google Scholar
  8. V. V. Shenoy, Z. Lwin, A. Morton, and J. Hardy, “Ectopic adrenocorticotrophic hormone syndrome associated with poor prognosis in metastatic parotid acinic cell carcinoma,” Otolaryngology—Head and Neck Surgery, vol. 145, no. 5, pp. 878–879, 2011. View at: Publisher Site | Google Scholar
  9. L. Jamieson, S. M. Taylor, A. Smith, M. J. Bullock, and M. Davis, “Metastatic acinic cell carcinoma of the parotid gland with ectopic ACTH syndrome,” Otolaryngology—Head and Neck Surgery, vol. 136, no. 1, pp. 149–150, 2007. View at: Publisher Site | Google Scholar
  10. V. Alcantara, E. Urgell, J. F. Sancho, and A. Chico, “Severe ectopic cushing syndrome caused by adenoid cystic carcinoma of a salivary gland,” Endocrine Practice, vol. 19, no. 5, pp. e118–e121, 2013. View at: Publisher Site | Google Scholar
  11. B. L. Wajchenberg, B. B. Mendonca, B. Liberman et al., “Ectopic adrenocorticotropic hormone syndrome,” Endocrine Reviews, vol. 15, no. 6, pp. 752–787, 1994. View at: Google Scholar
  12. J. P. Aniszewski, W. F. Young Jr., G. B. Thompson, C. S. Grant, and J. A. Van Heerden, “Cushing syndrome due to ectopic adrenocorticotropic hormone secretion,” World Journal of Surgery, vol. 25, no. 7, pp. 934–940, 2001. View at: Publisher Site | Google Scholar
  13. J. Newell-Price, P. Trainer, M. Besser, and A. Grossman, “The diagnosis and differential diagnosis of Cushing's syndrome and pseudo-Cushing's states,” Endocrine Reviews, vol. 19, no. 5, pp. 647–672, 1998. View at: Publisher Site | Google Scholar
  14. C. Invitti, F. P. Giraldi, M. de Martin, and F. Cavagnini, “Diagnosis and management of Cushing's syndrome: results of an Italian multicentre study. Study Group of the Italian Society of Endocrinology on the pathophysiology of the Hypothalamic-Pituitary-Adrenal axis,” The Journal of Clinical Endocrinology & Metabolism, vol. 84, no. 2, pp. 440–448, 1999. View at: Google Scholar
  15. D. C. Aron, H. Raff, and J. W. Findling, “Effectiveness versus efficacy: the limited value in clinical practice of high dose dexamethasone suppression testing in differential diagnosis of adrenocorticotropin-dependent Cushing`s syndrome,” Journal of Clinical Endocrinology and Metabolism, vol. 82, no. 6, pp. 1780–1785, 1997. View at: Google Scholar
  16. G. Reimondo, P. Paccotti, M. Minetto et al., “The corticotrophin-releasing hormone test is the most reliable non-invasive method to differentiate pituitary from ectopic ACTH secretion in Cushing's syndrome,” Clinical Endocrinology, vol. 58, no. 6, pp. 718–724, 2003. View at: Publisher Site | Google Scholar
  17. B. L. Wajchenberg, B. B. Mendonça, B. Liberman, M. A. A. Pereira, and M. A. Kirschner, “Ectopic ACTH syndrome,” The Journal of Steroid Biochemistry and Molecular Biology, vol. 53, no. 1–6, pp. 139–151, 1995. View at: Publisher Site | Google Scholar
  18. W. W. de Herder and S. W. J. Lamberts, “Tumor localization—the ectopic ACTH syndrome,” Journal of Clinical Endocrinology and Metabolism, vol. 84, no. 4, pp. 1184–1185, 1999. View at: Google Scholar
  19. P. M. Stewart, S. Gibson, S. R. Crosby et al., “ACTH precursors characterize the ectopic ACTH syndrome,” Clinical Endocrinology, vol. 40, no. 2, pp. 199–204, 1994. View at: Publisher Site | Google Scholar
  20. A. C. Hale, G. M. Besser, and L. H. Rees, “Characterization of pro-opiomelanocortin-derived peptides in pituitary and ectopic adrenocorticotrophin-secreting tumours,” Journal of Endocrinology, vol. 108, no. 1, pp. 49–56, 1986. View at: Publisher Site | Google Scholar
  21. T. Hara, H. Akutsu, T. Yamamoto, E. Ishikawa, M. Matsuda, and A. Matsumura, “Cushing's disease presenting with gastrointestinal perforation: a case report,” Endocrinology, Diabetes & Metabolism Case Reports, vol. 11, Article ID EDM130064, 2013. View at: Publisher Site | Google Scholar
  22. K. Piekarek and L. A. Israelsson, “Perforated colonic diverticular disease: the importance of NSAIDs, opioids, corticosteroids, and calcium channel blockers,” International Journal of Colorectal Disease, vol. 23, no. 12, pp. 1193–1197, 2008. View at: Publisher Site | Google Scholar
  23. P. J. Coates, I. Doniach, T. A. Howlett, L. H. Rees, and G. M. Besser, “Immunocytochemical study of 18 tumours causing ectopic Cushing's syndrome,” Journal of Clinical Pathology, vol. 39, no. 9, pp. 955–960, 1986. View at: Publisher Site | Google Scholar
  24. L. K. Nieman, B. M. Biller, J. W. Findling et al., “Treatment of Cushing's syndrome: an endocrine society clinical practice guideline,” The Journal of Clinical Endocrinology & Metabolism, vol. 100, no. 8, pp. 2807–2831, 2015. View at: Publisher Site | Google Scholar

Copyright © 2016 Thomas Dacruz et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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