Evidence map›Paper›PMID 36723686›Full record

ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2023

An adolescent case of sellar osteochondromyxoma in the setting of spondyloepiphyseal dysplasia.

Sophia Peng, Mandana Behbahani, Shelly Sharma, Nitin R Wadhwani, Jeff C Rastatter, Tord D Alden

Abstract readCase Reports
PubMed Publisher
In one paragraph

Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Sophia PengDepartment of Neurological Surgery, University of Illinois at Chicago, Chicago, IL, USA.
Mandana BehbahaniDivision of Neurosurgery, Ann and Robert H. Lurie Children's Hospital, 225 E. Chicago Ave, Box 28, Chicago, IL, 60611, USA.
Shelly SharmaDivision of Neurosurgery, Ann and Robert H. Lurie Children's Hospital, 225 E. Chicago Ave, Box 28, Chicago, IL, 60611, USA.
Nitin R WadhwaniDepartment of Pathology, Ann and Robert H. Lurie Children's Hospital, Chicago, IL, USA.
Jeff C RastatterDivision of Otolaryngology, Ann and Robert H. Lurie Children's Hospital, Chicago, IL, USA.
Tord D AldenDivision of Neurosurgery, Ann and Robert H. Lurie Children's Hospital, 225 E. Chicago Ave, Box 28, Chicago, IL, 60611, USA. TAlden@luriechildrens.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeOsteochondromyxomas (OMX) are rare congenital bone tumors that have only been described in the context of Carney complex syndrome (CNC). Data on OMX as a separate entity and in association with other disorders remain limited, making both diagnosis and treatment difficult.

methodsA case report of a 17-year-old female diagnosed with sellar OMX is presented in the setting of spondyloepiphyseal dysplasia (SED). We discuss the radiographic and histopathological interpretations in addition to reviewing the current literature on OMX.

resultsA successful gross total resection of the tumor was achieved via an endonasal endoscopic transsphenoidal approach. A diagnosis was established radiographically and pathologically.

conclusionThe diagnosis and treatment of OMX are best achieved via tissue biopsy. Following confirmed osteochondromyxoma cases long term for recurrence and outcomes will be essential in understanding its natural tumor history and in establishing standard treatments.

Indexed as

Bone NeoplasmsCartilage DiseasesMucopolysaccharidosis IVOsteochondrodysplasiasPituitary NeoplasmsSoft Tissue NeoplasmsAdolescentEndoscopyFemaleHumansTreatment OutcomeCase reportOsteochondromyxomaPediatric neurosurgerySpondyloepiphyseal dysplasia

Identifiers

PMID36723686

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.