 Myofibromatosis
"Myofibromatosis" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A condition characterized by multiple formations of myofibromas (LEIOMYOMA).
| Descriptor ID |
D018224
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| MeSH Number(s) |
C04.557.450.565.590.550
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Myofibromatosis".
Below are MeSH descriptors whose meaning is more specific than "Myofibromatosis".
This graph shows the total number of publications written about "Myofibromatosis" by people in this website by year, and whether "Myofibromatosis" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1999 | 1 | 0 | 1 | | 2018 | 1 | 0 | 1 | | 2021 | 1 | 0 | 1 | | 2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Myofibromatosis" by people in Profiles.
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Braun M, Pascual M, Mully T, Phelps A, Prok L, Shah SD, Kohn LL. Solitary cutaneous infantile myofibroma as a hallmark of myofibromatosis: Two cases and review of the literature. Pediatr Dermatol. 2022 May; 39(3):438-442.
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Szeto MD, Maymone MB, Kim LS, Bodmer J, Treece AL, Diaz-Miron JL. Infantile myofibromatosis: multiple firm nodules in a premature newborn. Dermatol Online J. 2021 Nov 15; 27(11).
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Al Qawahmed R, Sawyer SL, Vassilyadi M, Qin W, Boycott KM, Michaud J. Infantile Myofibromatosis With Intracranial Extradural Involvement and PDGFRB Mutation: A Case Report and Review of the Literature. Pediatr Dev Pathol. 2019 May-Jun; 22(3):258-264.
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Kasaragod AB, Lucia MS, Lum GM, Caldwell S, Stork L, Stenmark KR. Solitary renal myofibromatosis: an unusual cause of infantile hypertension. Pediatrics. 1999 May; 103(5):e66.
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