Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Albani, Adriana, Berr, Christina M., Beuschlein, Felix, Treitl, Marcus, Hallfeldt, Klaus, Honegger, Jürgen, Schnauder, Günter, Reincke, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
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
_version_ 1783461369860849664
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
work_keys_str_mv AT albaniadriana apitfallofbilateralinferiorpetrosalsinussamplingincycliccushingssyndrome
AT berrchristinam apitfallofbilateralinferiorpetrosalsinussamplingincycliccushingssyndrome
AT beuschleinfelix apitfallofbilateralinferiorpetrosalsinussamplingincycliccushingssyndrome
AT treitlmarcus apitfallofbilateralinferiorpetrosalsinussamplingincycliccushingssyndrome
AT hallfeldtklaus apitfallofbilateralinferiorpetrosalsinussamplingincycliccushingssyndrome
AT honeggerjurgen apitfallofbilateralinferiorpetrosalsinussamplingincycliccushingssyndrome
AT schnaudergunter apitfallofbilateralinferiorpetrosalsinussamplingincycliccushingssyndrome
AT reinckemartin apitfallofbilateralinferiorpetrosalsinussamplingincycliccushingssyndrome
AT albaniadriana pitfallofbilateralinferiorpetrosalsinussamplingincycliccushingssyndrome
AT berrchristinam pitfallofbilateralinferiorpetrosalsinussamplingincycliccushingssyndrome
AT beuschleinfelix pitfallofbilateralinferiorpetrosalsinussamplingincycliccushingssyndrome
AT treitlmarcus pitfallofbilateralinferiorpetrosalsinussamplingincycliccushingssyndrome
AT hallfeldtklaus pitfallofbilateralinferiorpetrosalsinussamplingincycliccushingssyndrome
AT honeggerjurgen pitfallofbilateralinferiorpetrosalsinussamplingincycliccushingssyndrome
AT schnaudergunter pitfallofbilateralinferiorpetrosalsinussamplingincycliccushingssyndrome
AT reinckemartin pitfallofbilateralinferiorpetrosalsinussamplingincycliccushingssyndrome