Neuroblastoma with opsomyoclonus and turner syndrome

Warrier, R. P.; Kini, Ratnakar; Besser, Arthur S.; D, Vandyke; Raju, Usha; Kottamasu, Sambasiva R.

doi:10.1007/bf02776630

Cited by 6 publications

(4 citation statements)

References 6 publications

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“…The association between the mean age of the Neuroblastoma patients and ophthalmologic manifestation according to our analysis of 65 case reports and Musarella et al8–10,12–14,16–18,21–37,44–73 HS indicates Horner syndrome; OMS, opsoclonus-myoclonus syndrome. *Statistical significance.…”

Section: Case Reports Analysismentioning

confidence: 87%

“…The incidence of the primary tumor localization in patients diagnosed with neuroblastoma, ganglioneuroblastoma, and ganglioneuroma according to the 84 analyzed case reports 9,10,12–14,16–18,21–31,33–39,44–53,55–62,64–66,68–79,81–84. AM indicates adrenal medulla; GN, ganglioneuroma; GNBL, ganglioneuroblastoma; NBL, neuroblastoma.…”

Section: Case Reports Analysismentioning

confidence: 99%

“…The incidence of opsoclonus-myoclonus syndrome and the associated symptoms in 68 children diagnosed with neuroblastoma, and 16 patients with ganglioneuroblastoma. Overall, there were 29 cases of opsoclonus-myoclonus syndrome 9,10,12–14,16–18,21–39,44–80. OMS indicates opsoclonus-myoclonus syndrome.…”

Section: Case Reports Analysismentioning

confidence: 99%

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Ophthalmologic Manifestations of Neuroblastoma: A Systemic Review

Kuchalska

Derwich²,

Gotz‐Więckowska

2022

Journal of Pediatric Hematology/Oncology

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Neuroblastoma (NBL) is the most common extracranial solid tumor found in pediatric patients. It develops from the sympathetic tract tissue. Although the symptoms are associated with tumor localization, sometimes NBL is manifested as ophthalmologic disorders. In this paper, we describe their incidence and the correlation with the prognosis. We searched 2 databases (PubMed and Web of Science) for papers published before April 2022, and concerned pediatric patients with NBL, which caused ophthalmologic changes. We collected 7 papers assessing the occurrence of ophthalmologic findings in the NBL patients, as well as 68 case reports presenting children with orbital changes and NBL, or with other tumors stemming from the sympathetic ganglia. The statistical analysis was performed to synthetize the data. The ophthalmologic signs occurred in 17.89% of the NBL cases; however, they were observed on presentation in 10.68%. The isolated ocular presentation was found in 2.56% of patients, whereas Horner syndrome was most frequent. The ophthalmologic symptoms correlated with patients’ age, primary tumor site, and survival rate. NBL may be challenging to diagnose in cases with isolated ophthalmologic manifestations. Numerous possible ocular signs can be observed, which emphasize the need for multidisciplinary care with regard to the NBL patients.

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Section: Case Reports Analysismentioning

confidence: 87%

Section: Case Reports Analysismentioning

confidence: 99%

See 1 more Smart Citation

Ophthalmologic Manifestations of Neuroblastoma: A Systemic Review

Kuchalska

Derwich²,

Gotz‐Więckowska

2022

Journal of Pediatric Hematology/Oncology

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“…This imaging confirmed local extension TS is a genetic disorder seen in females, characterised by partial or complete deletion of the X chromosome. The association between TS and neurogenic tumours has been reported in the literature, [1][2][3][4][5][6] however still lacks a definitive relationship. 2 This case is distinct, given the absence of clarity surrounding a final histopathological subtype and atypical nuclear medicine findings.…”

Section: E T T E R T O T H E E D I T O R a Unique Presentation Of Neu...mentioning

confidence: 99%