Evidence map›Paper›PMID 40804705›Full record

ArticlePediatric transplantation2025

Wandering Spleen in a Pediatric Lung Transplant Patient With Filamin A Deficiency: An Incidental Finding.

Savannah Ellis Knight, Mayel Yepez Donado, Maria Carolina Gazzaneo

Abstract readCase Reports
In one paragraph

Article in Pediatric transplantation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Savannah Ellis KnightDivision of Pediatric Pulmonary, Baylor College of Medicine/Texas Children's Hospital, Houston, Texas, USA.ORCID 0000-0001-5672-5893
Mayel Yepez DonadoDivision of Pediatric Pulmonary, Baylor College of Medicine/Texas Children's Hospital, Houston, Texas, USA.ORCID 0000-0001-7887-7513
Maria Carolina GazzaneoDivision of Pediatric Pulmonary and Critical Care, Baylor College of Medicine/Texas Children's Hospital, Houston, Texas, USA.ORCID 0000-0002-7495-0311

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFilamin A (FLNA) deficiency is a known cause of progressive lung disease and need for pediatric lung transplant; however, what may be less well known to lung transplant providers are the extrapulmonary complications of FLNA deficiencies, such as wandering spleen. We present a patient who underwent a lung transplant for FLNA deficiency and later developed posttransplant abdominal pain. CASE PRESENTATION: An 11-year-old female who had previously undergone a bilateral lung transplant due to FLNA deficiency, causing progressive lung disease, presented with abdominal pain and diarrhea. The patient's stool was tested for causes of gastroenteritis using a gastrointestinal pathogen panel (GIPP). Additionally, an initial abdominal ultrasound was obtained to rule out surgical causes of acute abdomen. The initial abdominal ultrasound showed the spleen in the correct anatomical location. However, subsequent abdominal ultrasounds revealed an incidental finding of wandering spleen in multiple locations in the abdomen. As she has remained stable despite the migration of her spleen, the decision was made not to pursue surgical intervention and to continue monitoring with medical and surgical follow-up.

conclusionsThere are multiple complications caused by FLNA deficiency besides progressive respiratory failure, which include gastrointestinal (GI) complications such as wandering spleen. Wandering spleen is a rare clinical entity and, to our knowledge, this is the first case report of it being identified in a pediatric lung transplant patient. This case highlights the importance of transplant providers remaining vigilant when evaluating seemingly benign complaints such as abdominal pain in this population.

Indexed as

FilaminsLung TransplantationPostoperative ComplicationsWandering SpleenChildFemaleHumansIncidental FindingsUltrasonographyFilaminsfilamin Apediatric lung transplantwandering spleen

Identifiers

PMID40804705
PMCPMC12350825

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