Evidence map›Paper›PMID 30131065›Full record

ArticleJournal of medical case reports2018

Diagnostic difficulties of primary angiosarcoma of the breast: a case report.

Youssef Mahdi, Lamiaa Rouas, Abderrahmane Malihy, Najat Lamalmi, Zaitouna Alhamany

Open access · goldAbstract readCase Reports
In one paragraph

Article in Journal of medical case reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 31% 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

4 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
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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

5 authors at 2 institutions in 1 country.

Youssef MahdiDepartment of Pathology, Gyneco-Obstetric and Pediatric Hospital, Ibn Sina University Hospital, Rabat, Morocco. ysf.mahdi@gmail.com.
Lamiaa RouasDepartment of Pathology, Gyneco-Obstetric and Pediatric Hospital, Ibn Sina University Hospital, Rabat, Morocco.
Abderrahmane MalihyDepartment of Pathology, Gyneco-Obstetric and Pediatric Hospital, Ibn Sina University Hospital, Rabat, Morocco.
Najat LamalmiDepartment of Pathology, Gyneco-Obstetric and Pediatric Hospital, Ibn Sina University Hospital, Rabat, Morocco.
Zaitouna AlhamanyDepartment of Pathology, Gyneco-Obstetric and Pediatric Hospital, Ibn Sina University Hospital, Rabat, Morocco.
Centre Hospitalier Ibn Sina · MAMohammed V University · MA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAngiosarcoma of the breast is a rare tumor, which may be primary or secondary to breast surgery or irradiation. It is characterized by polymorphic and nonspecific clinical and radiological features. A pathologist plays a key role in positive and differential diagnosis and in establishing the prognosis: only a histological examination can confirm the diagnosis, and the histologic grade is the most important prognostic factor. In fact, angiosarcomas of the breast constitute a very heterogeneous group and they are classified into three grades based on the degree of differentiation. We will illustrate diagnostic challenges through this new case of primary angiosarcoma of the breast. Microscopic findings were initially interpreted as a benign vascular tumor. We will also discuss the relevant medical literature. CASE PRESENTATION: A 56-year-old Arabian woman presented with a palpable right breast mass that had been enlarging for 2 months, measuring 5 cm, without axillary lymphadenopathy. She had no personal or family history of breast surgery or breast irradiation. A mammography showed no evidence of spiculation. No suspicious calcifications were seen. A needle core biopsy was performed. Microscopic findings were initially interpreted as a benign vascular tumor. However, as the mass measured 5 cm, the diagnosis of angiosarcoma was more appropriate, and mastectomy without axillary dissection was performed. Microscopic examination found mild to moderately scattered pleomorphic cells, and scattered mitotic figures. It also showed papillary formations, solid foci of spindle cells, and hemorrhagic necrosis. The margins of the tumor were infiltrative. The diagnosis of primary intermediately differentiated angiosarcoma of the breast (grade II) was made. No distant metastases were found. Our patient was lost to follow-up and further treatment after mastectomy until she developed local tumor progression 4 months later.

conclusionsThrough this case report, we emphasize the importance of clinicopathological confrontation in angiosarcoma of the breast.

Indexed as

Breast NeoplasmsFemaleHemangiosarcomaHumansMastectomyMiddle AgedPrognosisAngiosarcomaBreastCase reportPathology

Identifiers

PMID30131065
PMCPMC6103999
OpenAlexW2887877659

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.