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  1. Congenital epulis--a case report
    Ramanathan K, Karpal Singh
    Med J Malaysia, 1973 Sep;28(1):55-7.
    PMID: 4361092
    Matched MeSH terms: Neoplasms, Muscle Tissue/pathology*
  2. Alveolar soft part sarcoma: a case report
    Sengupta S, Murugasu R
    Med J Malaya, 1970 Sep;25(1):70-2.
    PMID: 4249502
    Matched MeSH terms: Neoplasms, Muscle Tissue/pathology*
  3. Metachronous inflammatory myofibroblastic tumour in the temporal bone: case report
    Goh BS, Tan SP, Husain S, Rose IM, Saim L
    J Laryngol Otol, 2009 Oct;123(10):1184-7.
    PMID: 19192318 DOI: 10.1017/S0022215109004642
    We report an extremely rare case of metachronous inflammatory myofibroblastic tumour in the temporal bone.
    Matched MeSH terms: Neoplasms, Muscle Tissue/pathology
  4. Myofibroblastoma of the breast
    Shanmugasiva VV, Ramli Hamid MT, Fadzli F, Shaleen Kaur KS, Abd Rahman N, Rahmat K
    Malays J Pathol, 2018 Dec;40(3):349-353.
    PMID: 30580368
    INTRODUCTION: Myofibroblastoma is a rare benign mesenchymal tumour arising from the stromal elements of the breast tissue. Histopathological variants such as classic, cellular, collagenous / fibrous, lipomatous, infiltrative, myxoid and epithelioid have been identified. Most myofibroblastomas are immunoreactive for CD34, actin, CD10 and desmin, usually express oestrogen receptor (ER), progesterone receptor (PR) and variably express androgen receptor (AR).

    CASE REPORT: We report a case of myofibroblastoma in an octogenarian male presenting with painless solitary breast lump. Mammography (digital tomosynthesis) and ultrasound showed a well-circumscribed hyperdense mass and hypoechoic, solid, oval mass with peripheral vascularity respectively. Patient underwent wide local excision.

    DISCUSSION: Diverse characteristics of myofibroblastoma on imaging necessitates histopathological analysis for an accurate diagnosis. Myofibroblastoma are often confused with fibroadenomas due to the benign imaging characteristics and with malignant neoplasia due to their wide morphological spectrum. Surgical excision is considered curative.

    Matched MeSH terms: Neoplasms, Muscle Tissue/pathology*
  5. An Obstructed Malignant Inflammatory Myofibroblastic Tumour of the Rectum
    Zainal Abidin ZA, Azizan N, Hayati F, Mra A, Mohd Azman ZA
    Kathmandu Univ Med J (KUMJ), 2018 7 1;16(63):272-274.
    PMID: 31719321
    Inflammatory myofibroblastic tumour is rare but more common in children. It shows an immunophenotypic features of myofibroblastic differentiation, hence bearing neoplastic potential. The diagnosis is challenging especially if it involves rectum. Surgical resection is the mainstay of treatment if clinically obstructed. A 65-year-old gentleman presented with intestinal obstruction, which then followed by a hartmann's procedure. Final diagnosis is a rare case of inflammatory myofibroblastic tumour of the rectum. We discuss its genetic involvement with a literature review.
    Matched MeSH terms: Neoplasms, Muscle Tissue/pathology
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