Publication Name	World Journal of Clinical Cases
Manuscript ID	91771
Country	Croatia

Received	2024-01-04 16:31
Peer-Review Started	2024-01-04 16:31
To Make the First Decision
Return for Revision	2024-01-17 02:08
Revised	2024-01-31 22:11
Second Decision	2024-03-15 02:35
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief	2024-03-15 07:45
Articles in Press	2024-03-15 07:45
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript	2024-03-25 08:33
Publish the Manuscript Online	2024-04-02 09:09

ISSN	2307-8960 (online)
Open Access	This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/
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Category	Oncology
Manuscript Type	Case Report
Article Title	Panhypopituitarism caused by a suprasellar germinoma: A case report
Manuscript Source	Invited Manuscript
All Author List	Jelena Roganovic, Lea Saric, Silvije Segulja, Ana Dordevic and Mia Radosevic
ORCID	Author(s) ORCID Number Jelena Roganovic http://orcid.org/0000-0002-7960-6069 Lea Saric http://orcid.org/0009-0001-5996-6147 Silvije Segulja http://orcid.org/0000-0002-2524-1324 Ana Dordevic http://orcid.org/0000-0003-3896-6698 Mia Radosevic http://orcid.org/0009-0003-8838-1521
Funding Agency and Grant Number
Corresponding Author	Jelena Roganovic, PhD, Adjunct Professor, Department of Pediatrics, Clinical Hospital Centre Rijeka, Istarska 43, Rijeka 51000, Croatia. roganovic.kbcri@gmail.com
Key Words	Germinoma; Germ cell tumor; Suprasellar tumor; Hypopituitarism; Management; Pediatrics; Case report
Core Tip	Suprasellar germinomas are rare tumors that may be associated with hypopituitarism at diagnosis and after therapy. We report the presentation, diagnosis, treatment, and complications of a suprasellar germinoma in a 12-year-old patient. The tumor caused visual impairment, headaches, and hypopituitarism. The patient was treated surgically, followed by adjuvant chemotherapy and radiotherapy. Post-treatment panhypopituitarism required hormonal replacement therapy. The case underscores the complexity of managing these rare tumors and the importance of a multidisciplinary approach. The findings contribute to the understanding of the long-term consequences and holistic lifelong care of pediatric patients with suprasellar germinomas.
Publish Date	2024-04-02 09:09
Citation	Roganovic J, Saric L, Segulja S, Dordevic A, Radosevic M. Panhypopituitarism caused by a suprasellar germinoma: A case report. World J Clin Cases 2024; 12(10): 1844-1850
URL	https://www.wjgnet.com/2307-8960/full/v12/i10/1844.htm
DOI	https://dx.doi.org/10.12998/wjcc.v12.i10.1844

Full Article (PDF)	WJCC-12-1844-with-cover.pdf
CARE Checklist–2016	91771-CARE Checklist (2016).pdf
Manuscript File	91771_Auto_Edited-YJP.docx
Answering Reviewers	91771-Answering reviewers.pdf
Audio Core Tip	91771-Audio core tip.m4a
Conflict-of-Interest Disclosure Form	91771-Conflict-of-interest statement.pdf
Copyright License Agreement	91771-Copyright license agreement.pdf
Signed Consent for Treatment Form(s) or Document(s)	91771-Informed consent statement.pdf
Non-Native Speakers of English Editing Certificate	91771-Language certificate.pdf
Peer-review Report	91771-Peer-review(s).pdf
Scientific Editor Work List	91771-Scientific editor work list.pdf