Exp Clin Endocrinol Diabetes 2011; 119(09): 525-529
DOI: 10.1055/s-0031-1284368
Case Report
© J. A. Barth Verlag in George Thieme Verlag KG Stuttgart · New York

Ectopic ACTH-syndrome due to a Neuroendocrine Tumour of the Appendix

N. Perakakis
1   Division of Endocrinology and Diabetology, Department of Internal Medicine II, University Hospital of Freiburg
,
K. Laubner
1   Division of Endocrinology and Diabetology, Department of Internal Medicine II, University Hospital of Freiburg
,
T. Keck
2   Department of General and Visceral Surgery, University Hospital of Freiburg
,
D. Steffl
3   Department of Nephrology, University Hospital of Freiburg
,
M. Lausch
3   Department of Nephrology, University Hospital of Freiburg
,
P. T. Meyer
4   Department of Nuclear Medicine, University Hospital of Freiburg
,
D. Burger
5   Department of Diagnostic Radiology, University Hospital of Freiburg
,
A. Csanadi
6   Institute of Pathology, University Hospital of Freiburg
,
J. Seufert
1   Division of Endocrinology and Diabetology, Department of Internal Medicine II, University Hospital of Freiburg
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Publikationsverlauf

received 16. Mai 2011
firstdecision 29. Juni 2011

accepted 12. Juli 2011

Publikationsdatum:
17. Oktober 2011 (online)

Abstract

Ectopic ACTH production causes 10% of Cushing’s syndromes. The diagnostic workup is difficult, can last more than 6 months (> 50% of cases), and the underlying tumour is still frequently not located (12%). Carcinoid tumours of the appendix are frequent and are revealed in 0.3% of patients undergoing routine appendectomy. However, neuroendocrine tumours of the appendix with ACTH production are an extremely rare entity.

Here we report the case of a female patient with clinically overt Cushing’s syndrome due to ectopic ACTH-production from a carcinoid tumour of the appendix. During the diagnostic workup, repeated endocrine tests, multiple different imaging modalities and frequent and lengthy hospitalisations were necessary. Wrongly, even a neurosurgical pituitary exploration was performed. After 12 months from the initial admission, the tumour was finally detected by an 18F-fluoro-L-dihydroxyphenylalanine (18FDOPA PET) and an appendectomy followed by right hemicolectomy were performed. The patient recovered rapidly and the symptoms from the hypercortisolism were no more present.

In this case, we discuss the multitude of problems, which may delay the diagnosis and the pitfalls, that should be avoided in order to locate the tumour and to initiate adequate therapy as early as possible. Furthermore, our case demonstrates the complexity of diagnostic procedures, which demand most of the times a multidisciplinary approach. In this setting, regular follow-ups in short time intervals and the use of novel imaging techniques can finally cut the diagnostic “Gordian knot”.

 
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