-
Je něco špatně v tomto záznamu ?
Ectopic adrenocorticotrophic hormone syndrome in a 10-year-old girl with a thymic neuroendocrine tumor: a case report
I. Aldhoon-Hainerová, M. Kosák, M. Kršek, D. Zogala, K. Pacak
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu kazuistiky, časopisecké články
NLK
BioMedCentral
od 2001-12-01
BioMedCentral Open Access
od 2001
Directory of Open Access Journals
od 2001
Free Medical Journals
od 2001
PubMed Central
od 2001
Europe PubMed Central
od 2001
ProQuest Central
od 2009-01-01
Open Access Digital Library
od 2001-10-01
Open Access Digital Library
od 2001-01-01
Open Access Digital Library
od 2001-01-01
Health & Medicine (ProQuest)
od 2009-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2001
Springer Nature OA/Free Journals
od 2001-12-01
- MeSH
- Cushingův syndrom etiologie diagnóza chirurgie MeSH
- dítě MeSH
- ektopický ACTH syndrom * diagnóza chirurgie MeSH
- ketokonazol terapeutické užití MeSH
- lidé MeSH
- nádory brzlíku * komplikace diagnóza chirurgie patologie MeSH
- neuroendokrinní nádory * komplikace diagnóza chirurgie patologie MeSH
- thymektomie MeSH
- Check Tag
- dítě MeSH
- lidé MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- kazuistiky MeSH
BACKGROUND: Thymic neuroendocrine tumor as a cause of Cushing syndrome is extremely rare in children. CASE PRESENTATION: We report a case of a 10-year-old girl who presented with typical symptoms and signs of hypercortisolemia, including bone fractures, growth retardation, and kidney stones. The patient was managed with oral ketoconazole, during which she experienced adrenal insufficiency, possibly due to either cyclic adrenocorticotropic hormone (ACTH) secretion or concurrent COVID-19 infection. The patient underwent a diagnostic work-up which indicated the possibility of an ACTH-secreting pituitary neuroendocrine tumor. However, after a transsphenoidal surgery, the diagnosis was not confirmed on histopathological examination. Subsequent bilateral inferior petrosal sinus sampling showed strong indications of the presence of ectopic ACTH syndrome. Detailed rereading of functional imaging studies, including 18F-FDG PET/MRI and 68Ga DOTATOC PET/CT, ultimately identified a small lesion in the thymus. The patient underwent videothoracoscopic thymectomy that confirmed a neuroendocrine tumor with ACTH positivity on histopathological examination. CONCLUSION: This case presents some unique challenges related to the diagnosis, management, and treatment of thymic neuroendocrine tumor in a child. We can conclude that ketoconazole treatment was effective in managing hypercortisolemia in our patient. Further, a combination of functional imaging studies can be a useful tool in locating the source of ectopic ACTH secretion. Lastly, in cases of discrepancy in the results of stimulation tests, bilateral inferior petrosal sinus sampling is highly recommended to differentiate between Cushing disease and ectopic ACTH syndrome.
3rd Department of Medicine 1st Faculty of Medicine Charles University Prague Czech Republic
Department of Medicine Military University Hospital Prague Czech Republic
Department of Pediatrics Thomayer University Hospital Prague Czech Republic
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc25003462
- 003
- CZ-PrNML
- 005
- 20250206104348.0
- 007
- ta
- 008
- 250121s2024 enk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1186/s12902-024-01756-5 $2 doi
- 035 __
- $a (PubMed)39538188
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a enk
- 100 1_
- $a Aldhoon-Hainerová, Irena $u Department of Children and Adolescents, Third Faculty of Medicine, Charles University, University Hospital Kralovske Vinohrady, Šrobárova 50, Prague, 100 34, Czech Republic. irena.aldhoon@fnkv.cz $u Department of Pediatrics, Thomayer University Hospital, Prague, Czech Republic. irena.aldhoon@fnkv.cz $1 https://orcid.org/0000000197839256
- 245 10
- $a Ectopic adrenocorticotrophic hormone syndrome in a 10-year-old girl with a thymic neuroendocrine tumor: a case report / $c I. Aldhoon-Hainerová, M. Kosák, M. Kršek, D. Zogala, K. Pacak
- 520 9_
- $a BACKGROUND: Thymic neuroendocrine tumor as a cause of Cushing syndrome is extremely rare in children. CASE PRESENTATION: We report a case of a 10-year-old girl who presented with typical symptoms and signs of hypercortisolemia, including bone fractures, growth retardation, and kidney stones. The patient was managed with oral ketoconazole, during which she experienced adrenal insufficiency, possibly due to either cyclic adrenocorticotropic hormone (ACTH) secretion or concurrent COVID-19 infection. The patient underwent a diagnostic work-up which indicated the possibility of an ACTH-secreting pituitary neuroendocrine tumor. However, after a transsphenoidal surgery, the diagnosis was not confirmed on histopathological examination. Subsequent bilateral inferior petrosal sinus sampling showed strong indications of the presence of ectopic ACTH syndrome. Detailed rereading of functional imaging studies, including 18F-FDG PET/MRI and 68Ga DOTATOC PET/CT, ultimately identified a small lesion in the thymus. The patient underwent videothoracoscopic thymectomy that confirmed a neuroendocrine tumor with ACTH positivity on histopathological examination. CONCLUSION: This case presents some unique challenges related to the diagnosis, management, and treatment of thymic neuroendocrine tumor in a child. We can conclude that ketoconazole treatment was effective in managing hypercortisolemia in our patient. Further, a combination of functional imaging studies can be a useful tool in locating the source of ectopic ACTH secretion. Lastly, in cases of discrepancy in the results of stimulation tests, bilateral inferior petrosal sinus sampling is highly recommended to differentiate between Cushing disease and ectopic ACTH syndrome.
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a dítě $7 D002648
- 650 12
- $a ektopický ACTH syndrom $x diagnóza $x chirurgie $7 D000182
- 650 12
- $a nádory brzlíku $x komplikace $x diagnóza $x chirurgie $x patologie $7 D013953
- 650 12
- $a neuroendokrinní nádory $x komplikace $x diagnóza $x chirurgie $x patologie $7 D018358
- 650 _2
- $a Cushingův syndrom $x etiologie $x diagnóza $x chirurgie $7 D003480
- 650 _2
- $a ketokonazol $x terapeutické užití $7 D007654
- 650 _2
- $a thymektomie $7 D013934
- 655 _2
- $a kazuistiky $7 D002363
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Kosák, Mikuláš $u Department of Medicine, Military University Hospital, Prague, Czech Republic
- 700 1_
- $a Kršek, Michal $u Third Department of Medicine, First Faculty of Medicine, Charles University, Prague, Czech Republic
- 700 1_
- $a Zogala, David $u Institute of Nuclear Medicine, First Faculty of Medicine, Charles University, General University Hospital, Prague, Czech Republic
- 700 1_
- $a Pacak, Karel $u Developmental Endocrinology, Metabolism, Genetics and Endocrine Oncology Affinity Group, Eunice Kennedy Shriver NICHD, NIH, Bethesda, MD, USA
- 773 0_
- $w MED00006837 $t BMC endocrine disorders $x 1472-6823 $g Roč. 24, č. 1 (2024), s. 243
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/39538188 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y - $z 0
- 990 __
- $a 20250121 $b ABA008
- 991 __
- $a 20250206104343 $b ABA008
- 999 __
- $a ok $b bmc $g 2263313 $s 1239469
- BAS __
- $a 3
- BAS __
- $a PreBMC-MEDLINE
- BMC __
- $a 2024 $b 24 $c 1 $d 243 $e 20241113 $i 1472-6823 $m BMC endocrine disorders $n BMC Endocr Disord $x MED00006837
- LZP __
- $a Pubmed-20250121