Evidence map›Paper›PMID 37908610›Full record

ArticleBioinformation2023

Diversity of small round cell sarcoma in soft tissues around bone among Indian patients.

Rani Singh Guddi, Kumari Bharti, Anuja Mishra, Dinesh Kumar Sinha, Debaditya Haldar, Shabana Azad

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Article in Bioinformation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
–field-weighted citation impact, top 66% of its field
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

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3 · Its place in the literature

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0 citing papers in PubMed, 0 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Rani Singh GuddiDepartment of Pathology, Indira Gandhi Institute of Medical Sciences, Bihar, India.
Kumari BhartiDepartment of Pathology, Indira Gandhi Institute of Medical Sciences, Bihar, India.
Anuja MishraPathologyConsultant Pathologist, Indira Pathlabs (A unit of Indira IVF Pvt. Ltd.), Patna, Bihar, India.
Dinesh Kumar SinhaDepartment of Radiation Oncology, Indira Gandhi Institute of Medical Sciences, Bihar, India.
Debaditya HaldarDepartment of Pathology, IGIMS, Patna, Bihar, India.
Shabana AzadOncopathology, Homi Bhabha Cancer Hospital, Varanasi, Uttar Pradesh, India.
Indira Gandhi Institute of Medical Sciences · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Round cell tumors are a group of malignant tumors which shows overlapping microscopic features of small round monotonous cells with hyper-chromatic nucleus. It mostly occurs in children, adolescent, and young adults. The ancillary technique to confirm the differential diagnosis of round cells sarcoma is immuno-histo chemistry (IHC). Therefore, it is of interest to document the diversity of small round cell sarcoma in soft tissues around bones among Indian patients using IHC. A total of 334 cases among Indians were studied. Among them 160 cases were Non-Hodgkin's Lymphoma, 82 cases are poorly differentiated carcinoma and 92 cases of round cell sarcoma. Out of 92 cases, there were (40%) 27 cases of Wilms tumour, with the highest incidence. The highest incidence was observed in 0-14 years of age group with highest incidence in males. The distribution and diverse histology of different small round cell sarcoma offers challenge in the diagnosis by histopathology. Most frequent round cell tumour is Wilms tumour, followed by Rhabdomyosarcoma. Data shows the role of IHC in classifying soft tissue sarcoma but some time result of IHC remains inconclusive, where cytogenetic is important.

Indexed as

immune histochemistrySmall round cell sarcomatumor

Identifiers

PMID37908610
PMCPMC10613818
OpenAlexW4386983000

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