Evidence map›Paper›PMID 40392511›Full record

ReviewAmerican journal of clinical dermatology2025

Mastocytosis in the Skin: Approach to Diagnosis, Evaluation, and Management in Adult and Pediatric Patients.

Lauren M Madigan, Nathan A Boggs, Anton V Rets, Alejandro A Gru, Tsewang Tashi, David A Wada, Scott R Florell, Melody C Carter

Erratum issuedAbstract readReview
In one paragraph

Review in American journal of clinical dermatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Lauren M MadiganDepartment of Dermatology, University of Utah Health, HELIX Building Level 1 South, 30 N. Mario Capecchi Drive, Salt Lake City, UT, 84112, USA. lauren.madigan@hsc.utah.edu.ORCID http://orcid.org/0000-0001-5659-5734
Nathan A BoggsAllergy and Immunology Service, Walter Reed National Military Medical Center, Bethesda, MD, USA.
Anton V RetsARUP Laboratories, Salt Lake City, UT, USA.
Alejandro A GruDepartment of Dermatology, Columbia University, New York City, NY, USA.
Tsewang TashiDivision of Hematology, University of Utah School of Medicine, Salt Lake City, UT, USA.
David A WadaDepartment of Dermatology, University of Utah Health, HELIX Building Level 1 South, 30 N. Mario Capecchi Drive, Salt Lake City, UT, 84112, USA.
Scott R FlorellDepartments of Dermatology, and Pathology, University of Utah School of Medicine, Salt Lake City, UT, USA.
Melody C CarterLaboratory of Allergic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mastocytosis is characterized by the clonal infiltration and proliferation of neoplastic mast cells into target organs. Clinical features of mastocytosis are based in large part on dysregulated mast cell mediator release. Affected individuals may present with isolated skin involvement or multisystemic disease with a spectrum of symptoms including anaphylaxis, pathologic fractures, and chronic gastrointestinal, neurocognitive, musculoskeletal, and constitutional symptoms. The term "mastocytosis in the skin" refers to individuals with cutaneous infiltration and encompasses both localized and systemic forms of disease. Cutaneous involvement is further categorized into cutaneous mastocytoma, diffuse cutaneous mastocytosis, and maculopapular cutaneous mastocytosis based on morphology. In ~95% of patients with systemic mastocytosis, the disease is driven by the KIT D816V somatic variant. The aim of this clinical review is to highlight the diagnostic considerations, management complexities, and evolving treatment landscape that must be considered when evaluating a patient presenting with mastocytosis in their skin. Clinical manifestations, histopathology, and laboratory parameters are essential to diagnosis and determining the disease burden in those with known or suspected systemic mastocytosis. Once appropriately staged, both skin-directed therapy as well as novel systemic treatment options, including selective tyrosine kinase inhibitors, can be considered with the potential to improve patient outcomes.

Indexed as

Mastocytosis, CutaneousMastocytosis, SystemicSkinAdultChildDiagnosis, DifferentialHumansMast CellsProtein Kinase InhibitorsProto-Oncogene Proteins c-kitKIT protein, humanProtein Kinase InhibitorsProto-Oncogene Proteins c-kit

Identifiers

PMID40392511
PMCPMC12325572

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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.