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Dwarfism associated with wandering splenomegaly

Dwarfism associated with splenomegaly during teenage years is known. The purpose of this report was to present the first case of dwarfism associated with wandering splenomegaly. A 14-year-old boy presented a wandering splenomegaly and torsion of the splenic pedicle associated with a retarded growth...

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Autores principales: Petroianu, Andy, Sabino, Kelly Renata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8784172/
https://www.ncbi.nlm.nih.gov/pubmed/35079332
http://dx.doi.org/10.1093/jscr/rjab558
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author Petroianu, Andy
Sabino, Kelly Renata
author_facet Petroianu, Andy
Sabino, Kelly Renata
author_sort Petroianu, Andy
collection PubMed
description Dwarfism associated with splenomegaly during teenage years is known. The purpose of this report was to present the first case of dwarfism associated with wandering splenomegaly. A 14-year-old boy presented a wandering splenomegaly and torsion of the splenic pedicle associated with a retarded growth and sexual underdevelopment characterized by lack of sexual maturity and absence of secondary sexual physical appearance. The patient was submitted to detorsion of the spleen, and splenopexy. After the surgery, the patient grew up, and his sexual characteristics developed to normal. The size of the spleen reduced from the 22 × 16 × 13 cm to 14 × 12 × 10 cm after the surgical procedure. This is the first report of dwarfism associated with wandering splenomegaly, which was successfully treated without partial or total splenectomy. After releasing the venous blood flow, the spleen reduced its dimension and the patient grew up to the expected family size.
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spelling pubmed-87841722022-01-24 Dwarfism associated with wandering splenomegaly Petroianu, Andy Sabino, Kelly Renata J Surg Case Rep Case Report Dwarfism associated with splenomegaly during teenage years is known. The purpose of this report was to present the first case of dwarfism associated with wandering splenomegaly. A 14-year-old boy presented a wandering splenomegaly and torsion of the splenic pedicle associated with a retarded growth and sexual underdevelopment characterized by lack of sexual maturity and absence of secondary sexual physical appearance. The patient was submitted to detorsion of the spleen, and splenopexy. After the surgery, the patient grew up, and his sexual characteristics developed to normal. The size of the spleen reduced from the 22 × 16 × 13 cm to 14 × 12 × 10 cm after the surgical procedure. This is the first report of dwarfism associated with wandering splenomegaly, which was successfully treated without partial or total splenectomy. After releasing the venous blood flow, the spleen reduced its dimension and the patient grew up to the expected family size. Oxford University Press 2022-01-22 /pmc/articles/PMC8784172/ /pubmed/35079332 http://dx.doi.org/10.1093/jscr/rjab558 Text en Published by Oxford University Press and JSCR Publishing Ltd. All rights reserved. © The Author(s) 2022. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Petroianu, Andy
Sabino, Kelly Renata
Dwarfism associated with wandering splenomegaly
title Dwarfism associated with wandering splenomegaly
title_full Dwarfism associated with wandering splenomegaly
title_fullStr Dwarfism associated with wandering splenomegaly
title_full_unstemmed Dwarfism associated with wandering splenomegaly
title_short Dwarfism associated with wandering splenomegaly
title_sort dwarfism associated with wandering splenomegaly
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8784172/
https://www.ncbi.nlm.nih.gov/pubmed/35079332
http://dx.doi.org/10.1093/jscr/rjab558
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