Evidence map›Paper›PMID 35165585›Full record

ArticleCureus2022

Unicentric Castleman Disease With Systemic Symptoms: A Rare Case From Family Practice.

Amjad K Aljuaid, Moayad N Iskandar, Abdullah A Almalki, Khalifah S Alsuqayh, Yahya A Almufarrih, Saud G Alosaimi, Lamis F Aljamaan, Saad F Aldaihani, Sarah A Alghamdi, Mohammed A Alaamree and 5 more

RetractedOpen access · diamondAbstract readCase ReportsRetracted Publication
In one paragraph

Article in Cureus, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 99% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 6 institutions in 2 countries.

Amjad K AljuaidCollege of Medicine, Umm Al-Qura University, Mecca, SAU.
Moayad N IskandarCollege of Medicine, Umm Al-Qura University, Mecca, SAU.
Abdullah A AlmalkiCollege of Medicine, Umm Al-Qura University, Mecca, SAU.
Khalifah S AlsuqayhPediatric Surgery Department, Maternity and Children Hospital, Qassim, SAU.
Yahya A AlmufarrihCollege of Medicine, Majmaah University, Al-Majma'ah, SAU.
Saud G AlosaimiCollege of Medicine, Taif University, Taif, SAU.
Lamis F AljamaanCollege of Medicine, King Faisal University, Hofuf, SAU.
Saad F AldaihaniCollege of Medicine, University of Malta, Msida, SAU.
Sarah A AlghamdiCollege of Medicine, King Abdulaziz University, Jeddah, SAU.
Mohammed A AlaamreeCollege of Medicine, King Khalid University, Abha, SAU.
Lamees M FageehCollege of Medicine, King Khalid University, Abha, SAU.
Sara A AlmagrafiCollege of Medicine, King Khalid University, Abha, SAU.
Ali Y Al HalbubCollege of Medicine, King Khalid University, Abha, SAU.
Zoha S AlghamdiCollege of Medicine, King Khalid University, Abha, SAU.
Faisal Al-HawajCollege of Medicine, Imam Abdulrahman Bin Faisal University, Dammam, SAU.
King Faisal University · SAMajmaah University · SAKing Khalid University · SATaif University · SAMaternity and Children's Hospital · SAUmm al-Qura University · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Palpable lymphadenopathy is very common in children. The vast majority of cases are due to benign conditions and self-limiting diseases. Careful clinical evaluation, with thorough history taking and make a comprehensive physical examination, is essential to avoid unnecessary invasive procedures and not to misdiagnose possible serious underlying conditions. We report the case of a 9-year-old child with a lump in the right axilla that was first noticed with a swelling two months ago. The lump was not painful but its size has been gradually increasing. The symptom was associated with night sweats. However, there was no history of cough, fever, or weight loss. The child had no history of animal contact or insect bites. No recent travel or history of contact with any sick person was reported. His vaccination schedule was up-to-date. Upon examination, the patient had a smooth non-tender swelling in the right axilla. It measured around 4 x 4 cm. The overlying skin was normal with no erythema or ulceration. The swelling was mobile and was not adherent to the overlying skin. Laboratory investigation showed mild anemia, thrombocytosis, and elevated C-reactive protein level. An ultrasound examination demonstrated a well-circumscribed enlarged lymph node, measuring 3.4 cm in short axis, with an increased blood flow on color doppler. Biopsy findings showed proliferation of the follicular lymphoid tissues that were centered around penetrative vessels giving the appearance of "onion skin" in keeping with Castleman disease. Complete surgical resection of the lymph node was performed and resulted in the resolution of the systemic symptoms. Castleman disease is a rare lymphoproliferative disorder with shared histopathological features. Unicentric Castleman disease usually presents with isolated asymptomatic lymphadenopathy. However, the present case demonstrated that patients with unicentric Castleman disease may exhibit systemic constitutional symptoms similar to that of the multicentric subtype.

Indexed as

case reportcastleman diseaselymphadenopathylymphoproliferative disodernight sweats

Identifiers

PMID35165585
PMCPMC8831318
OpenAlexW4205764689

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.