Evidence map›Paper›PMID 40177159›Full record

ArticleClinical case reports2025

Hyperparathyroidism-Jaw Tumor Syndrome: A Rare Case Report and Literature Review.

Maria Memon, Nouman Ibrahim, Muhammad Momin Khan, Aakash Rai Khatri, Mahesh Kumar Meghwar, Farina Fatima Siddiqui, Maisam Ali Rajput, Alaa Jlailati

Abstract read
In one paragraph

Article in Clinical case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Diagnostic Dilemma Involving a Rare Case of aAACE endocrinology and diabetes
    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

8 authors.

Maria MemonDepartment of General Surgery Liaquat University Hospital Hyderabad Pakistan.
Nouman IbrahimDepartment of General Surgery Liaquat University Hospital Hyderabad Pakistan.
Muhammad Momin KhanDepartment of Internal Medicine Liaquat University Hospital Hyderabad Pakistan.
Aakash Rai KhatriDepartment of General Surgery Liaquat University Hospital Hyderabad Pakistan.
Mahesh Kumar MeghwarDepartment of General Surgery Liaquat University Hospital Hyderabad Pakistan.
Farina Fatima SiddiquiDepartment of Internal Medicine Liaquat University Hospital Hyderabad Pakistan.ORCID https://orcid.org/0009-0009-8893-0328
Maisam Ali RajputDepartment of Internal Medicine Liaquat University Hospital Hyderabad Pakistan.
Alaa JlailatiFaculty of Medicine, Department of Medicine Damascus University Damascus Syria.ORCID https://orcid.org/0009-0004-3848-1097

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prompt identification of Hyperparathyroidism-Jaw Tumor Syndrome (HPT-JT) is vital, particularly for those with a family history or unusual symptoms like progressive facial changes. By employing a thorough diagnostic strategy that includes biochemical tests, imaging, and genetic analysis, we can achieve early diagnosis and effective intervention. In this case, the patient displayed maxillofacial tumors, hypercalcemia, and increased parathyroid hormone levels. Imaging confirmed a parathyroid adenoma, while histopathology showed characteristics of brown tumors. Subtotal parathyroidectomy is the recommended treatment. Additionally, regular follow-ups every 6 months involving biochemical tests and imaging are crucial for ensuring the best patient outcomes.

Indexed as

Brown tumorgenetic mutationhyperparathyroidismuterine tumor

Identifiers

PMID40177159
PMCPMC11961338

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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.