Evidence map›Paper›PMID 25685570›Full record

ArticleCase reports in obstetrics and gynecology2015

Primary vaginal myeloid sarcoma: a rare case report and review of the literature.

Gaurang Modi, Irappa Madabhavi, Harsha Panchal, Apurva Patel, Asha Anand, Sonia Parikh, Pritam Jain, Swaroop Revannasiddaiah, Malay Sarkar

Open access · goldAbstract read
In one paragraph

Article in Case reports in obstetrics and gynecology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

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

11 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Erythroblastic sarcoma in the thoracic cavity of a cow.The Journal of veterinary medical science · 2019
    Article
  8. Primary Vaginal Chloroma: A Rare Case Report.International journal of hematology-oncology and stem cell research · 2018
    Article
  9. Article
  10. Article
  11. 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

9 authors at 2 institutions in 1 country.

Gaurang ModiDepartment of Medical and Paediatric Oncology, GCRI, Ahmedabad, Gujarat, India.
Irappa MadabhaviDepartment of Medical and Paediatric Oncology, GCRI, Ahmedabad, Gujarat, India.ORCID 0000-0002-8543-2413
Harsha PanchalDepartment of Medical and Paediatric Oncology, GCRI, Ahmedabad, Gujarat, India.
Apurva PatelDepartment of Medical and Paediatric Oncology, GCRI, Ahmedabad, Gujarat, India.
Asha AnandDepartment of Medical and Paediatric Oncology, GCRI, Ahmedabad, Gujarat, India.
Sonia ParikhDepartment of Medical and Paediatric Oncology, GCRI, Ahmedabad, Gujarat, India.
Pritam JainDepartment of Medical and Paediatric Oncology, GCRI, Ahmedabad, Gujarat, India.
Swaroop RevannasiddaiahDepartment of Radiotherapy, Government Medical College, Haldwani, India.
Malay SarkarDepartment of Pulmonary Medicine, IGMC, Shimla, Himachal Pradesh, India.
Gujarat Cancer & Research Institute · INGovernment Medical College · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myeloid sarcoma (chloroma, granulocytic sarcoma, or extramedullary myeloid tumour) is an extramedullary mass forming neoplasm composed of myeloid precursor cells. It is usually associated with myeloproliferative disorders but very rarely may precede the onset of leukemia. Here, we are presenting a rare case of primary vaginal myeloid sarcoma in a geriatric female patient without initial presentation of acute myeloid leukemia (AML). A 68-year-old female patient with ECOG Performance Score of 1 presented with pervaginal bleeding for 20 days. On colposcopic examination, she was found to have mass in the anterior fornix of vagina. A punch biopsy specimen revealed chloromatous infiltration of the vagina. LCA (leukocyte common antigen), MPO (myeloperoxidase), and c-kit were strongly positive on IHC (immunohistochemistry). The patient's routine blood investigations were normal including peripheral smear, lactose dehydrogenase, uric acid, 2D echocardiography, conventional cytogenetics, bone marrow aspiration, and biopsy. The patient was given 4 cycles of decitabine (Decitex, manufactured by Sun Pharmaceutical Industries Limited, India), 20 mg/m(2) for 5 days at an interval of 28 days. There was a partial response to decitabine according to RECIST criteria. As decitabine therapy was well tolerated, we are continuing in the same way until disease progression without any complications. The patient is undergoing regular follow-up at our centre.

Identifiers

PMID25685570
PMCPMC4313514
OpenAlexW2084277405

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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.