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A pitfall of bilateral inferior petrosal sinus sampling in cyclic Cushing’s syndrome
BACKGROUND: Clinical care of patients with cyclic Cushing’s syndrome (CS) is challenging. Classical pitfalls include incorrect subtyping, unnecessary surgical procedures and delayed definite treatment. CASE PRESENTATION: A 43-year-old female suffered from a rapidly cycling ectopic CS. She experience...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6805379/ https://www.ncbi.nlm.nih.gov/pubmed/31640675 http://dx.doi.org/10.1186/s12902-019-0433-9 |
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author | Albani, Adriana Berr, Christina M. Beuschlein, Felix Treitl, Marcus Hallfeldt, Klaus Honegger, Jürgen Schnauder, Günter Reincke, Martin |
author_facet | Albani, Adriana Berr, Christina M. Beuschlein, Felix Treitl, Marcus Hallfeldt, Klaus Honegger, Jürgen Schnauder, Günter Reincke, Martin |
author_sort | Albani, Adriana |
collection | PubMed |
description | BACKGROUND: Clinical care of patients with cyclic Cushing’s syndrome (CS) is challenging. Classical pitfalls include incorrect subtyping, unnecessary surgical procedures and delayed definite treatment. CASE PRESENTATION: A 43-year-old female suffered from a rapidly cycling ectopic CS. She experienced six cycles of severe hypercortisolism within a 2 year period (maximum plasma cortisol 5316 nmol/L, normal range 124.2–662.4 nmol/L; maximum urinary free cortisol 79,469 nmol/24 h, normal range < 414 nmol/24 h) lasting 2–9 weeks. The episodes were associated with pronounced hypokalemia (lowest K(+) value recorded 2.4 mmol/l) and progressive signs and symptoms of CS. A bilateral inferior petrosal sinus sampling (BIPSS) performed during a trough phase was false positive for pituitary ACTH overproduction resulting in unnecessary transsphenoidal surgery while a second BIPSS performed during an active phase was indicative for ectopic CS. The (18)F-DOPA PET/CT showed a pancreatic lesion, which was subsequently partially removed. Surprisingly, the histopathology was conclusive for ACTH-positive lymph node metastasis located in the retro-duodenal tissue of an occult neuroendocrine tumor WHO grade II. The primary tumor has not been identified so far and, because of the persistent hypercortisolism, the patient underwent bilateral adrenalectomy. Two years later, ACTH levels started to increase progressively. Percutaneous biopsy of a newly identified suspected lesion in the fifth thoracic vertebra revealed a metastasis with positive staining for ACTH, synaptophysin and chromogranin A. Therapy with carboplatin and etoposide was started and, since then, the patient underwent 12 cycles of chemotherapy. CONCLUSIONS: We report the challenging case of a rapidly cycling CS secondary to ACTH-secreting neuroendocrine intestinal tumor of unknown primary. We highlight the importance of performing diagnostic tests only during the phases of active cortisol secretion and as soon as first symptoms appear to avoid pitfalls. |
format | Online Article Text |
id | pubmed-6805379 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-68053792019-10-24 A pitfall of bilateral inferior petrosal sinus sampling in cyclic Cushing’s syndrome Albani, Adriana Berr, Christina M. Beuschlein, Felix Treitl, Marcus Hallfeldt, Klaus Honegger, Jürgen Schnauder, Günter Reincke, Martin BMC Endocr Disord Case Report BACKGROUND: Clinical care of patients with cyclic Cushing’s syndrome (CS) is challenging. Classical pitfalls include incorrect subtyping, unnecessary surgical procedures and delayed definite treatment. CASE PRESENTATION: A 43-year-old female suffered from a rapidly cycling ectopic CS. She experienced six cycles of severe hypercortisolism within a 2 year period (maximum plasma cortisol 5316 nmol/L, normal range 124.2–662.4 nmol/L; maximum urinary free cortisol 79,469 nmol/24 h, normal range < 414 nmol/24 h) lasting 2–9 weeks. The episodes were associated with pronounced hypokalemia (lowest K(+) value recorded 2.4 mmol/l) and progressive signs and symptoms of CS. A bilateral inferior petrosal sinus sampling (BIPSS) performed during a trough phase was false positive for pituitary ACTH overproduction resulting in unnecessary transsphenoidal surgery while a second BIPSS performed during an active phase was indicative for ectopic CS. The (18)F-DOPA PET/CT showed a pancreatic lesion, which was subsequently partially removed. Surprisingly, the histopathology was conclusive for ACTH-positive lymph node metastasis located in the retro-duodenal tissue of an occult neuroendocrine tumor WHO grade II. The primary tumor has not been identified so far and, because of the persistent hypercortisolism, the patient underwent bilateral adrenalectomy. Two years later, ACTH levels started to increase progressively. Percutaneous biopsy of a newly identified suspected lesion in the fifth thoracic vertebra revealed a metastasis with positive staining for ACTH, synaptophysin and chromogranin A. Therapy with carboplatin and etoposide was started and, since then, the patient underwent 12 cycles of chemotherapy. CONCLUSIONS: We report the challenging case of a rapidly cycling CS secondary to ACTH-secreting neuroendocrine intestinal tumor of unknown primary. We highlight the importance of performing diagnostic tests only during the phases of active cortisol secretion and as soon as first symptoms appear to avoid pitfalls. BioMed Central 2019-10-22 /pmc/articles/PMC6805379/ /pubmed/31640675 http://dx.doi.org/10.1186/s12902-019-0433-9 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Albani, Adriana Berr, Christina M. Beuschlein, Felix Treitl, Marcus Hallfeldt, Klaus Honegger, Jürgen Schnauder, Günter Reincke, Martin A pitfall of bilateral inferior petrosal sinus sampling in cyclic Cushing’s syndrome |
title | A pitfall of bilateral inferior petrosal sinus sampling in cyclic Cushing’s syndrome |
title_full | A pitfall of bilateral inferior petrosal sinus sampling in cyclic Cushing’s syndrome |
title_fullStr | A pitfall of bilateral inferior petrosal sinus sampling in cyclic Cushing’s syndrome |
title_full_unstemmed | A pitfall of bilateral inferior petrosal sinus sampling in cyclic Cushing’s syndrome |
title_short | A pitfall of bilateral inferior petrosal sinus sampling in cyclic Cushing’s syndrome |
title_sort | pitfall of bilateral inferior petrosal sinus sampling in cyclic cushing’s syndrome |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6805379/ https://www.ncbi.nlm.nih.gov/pubmed/31640675 http://dx.doi.org/10.1186/s12902-019-0433-9 |
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