-
Acta Clinica Croatica Mar 2019A case is presented of upper lip angiomyoma in a 36-year-old man. The tumor was painless, palpable and clinically visible. The operation was performed under local... (Review)
Review
A case is presented of upper lip angiomyoma in a 36-year-old man. The tumor was painless, palpable and clinically visible. The operation was performed under local anesthesia in the Outpatient Department. There were no complications during the postoperative course. Current literature on the subject is listed in the introduction, followed by presentation of the case and histologic characteristics of the tumor. This case is described as one of the differential diagnostic possibilities in the diagnosis of soft tissue tumors of the lip. Also, through review of the literature, different clinical appearances of angiomyoma, histologic variations and immunohistochemical characteristics are discussed that can help identify this tumor.
Topics: Adult; Angiomyoma; Biopsy; Diagnosis, Differential; Humans; Lip Neoplasms; Male; Treatment Outcome
PubMed: 31363342
DOI: 10.20471/acc.2019.58.01.24 -
Orthopedics Dec 1988Angiomyoma of the upper extremities is not commonly encountered by the orthopedic surgeon. A case of a vascular leiomyoma developing in a 79-year-old woman is discussed... (Review)
Review
Angiomyoma of the upper extremities is not commonly encountered by the orthopedic surgeon. A case of a vascular leiomyoma developing in a 79-year-old woman is discussed along with a review of the literature.
Topics: Aged; Female; Hand; Hemangioma; Humans; Leiomyoma
PubMed: 3068651
DOI: 10.3928/0147-7447-19881201-12 -
Cancer Genetics and Cytogenetics Aug 1996A t(X;10)(q22;q23.2) translocation was detected as the only chromosomal aberration in primary short-term cultured cells from an angiomyoma of a 58-year-old woman; 6p,... (Review)
Review
A t(X;10)(q22;q23.2) translocation was detected as the only chromosomal aberration in primary short-term cultured cells from an angiomyoma of a 58-year-old woman; 6p, 13q, and 21q rearrangements have been previously demonstrated by others in two cases of angiomyoma. This type of translocation has not been reported in other benign tumors including leiomyomas and angiomyomas, although it has been detected in an ependymoma. This is thought to be a third case of angiomyoma showing karyotypic abnormalities.
Topics: Angiomyoma; Chromosomes, Human, Pair 10; Female; Fingers; Humans; Karyotyping; Middle Aged; X Chromosome
PubMed: 8780748
DOI: 10.1016/0165-4608(96)00070-2 -
The Journal of Craniofacial Surgery Sep 2010Angiomyoma is a rare benign tumor originated from vascular smooth muscle cells, in other words, the tunica media, and the characteristic is the detection of numerous... (Review)
Review
Angiomyoma is a rare benign tumor originated from vascular smooth muscle cells, in other words, the tunica media, and the characteristic is the detection of numerous blood vessels together with spindle-shape smooth muscle cells. In most cases, it occurs in the subcutaneous tissue of the limbs, especially in the lower limbs, but it is very rare that it occurs in the head and neck area. In the head and neck area, it is developed most frequently in the larynx and the turbinates, and in addition, the development in the oral cavity (lip, hard palate, tonsil), nose, ear, cheek, parotid gland, and submandibular region has been reported. To the best of our knowledge, this is the first case report of angiomyoma that developed in the buccal space and some reviews of the literature.
Topics: Angiomyoma; Diagnosis, Differential; Humans; Male; Middle Aged; Mouth Neoplasms; Tomography, X-Ray Computed
PubMed: 20856064
DOI: 10.1097/SCS.0b013e3181ef67f1 -
Dento Maxillo Facial Radiology Oct 2010Angiomyomas of the oral cavity are rare benign vascular neoplasms. In particular, the congenital form has not been reported before in the English language literature. We... (Review)
Review
Angiomyomas of the oral cavity are rare benign vascular neoplasms. In particular, the congenital form has not been reported before in the English language literature. We present a congenital angiomyoma of the tongue that was found on the posterior middle of the tongue in an infant. On MRI, the mass showed an isointense signal to muscle on the T₁ weighted image and a slightly hyperintense signal on the T₂ weighted image. Immunohistochemically, tumour cells were positive to desmin and smooth muscle actin, but negative to vimentin and S100. The treatment was surgical excision and no recurrence was found during the 26 month follow-up period.
Topics: Actins; Angiomyoma; Desmin; Humans; Infant; Magnetic Resonance Imaging; Tongue Neoplasms
PubMed: 20841464
DOI: 10.1259/dmfr/32524441 -
Journal of Oral and Maxillofacial... Apr 2000
Review
Topics: Angiomyoma; Child; Diagnosis, Differential; Facial Pain; Humans; Lip Neoplasms; Male
PubMed: 10759131
DOI: 10.1016/s0278-2391(00)90935-2 -
The Journal of Urology Oct 1998
Review
Topics: Adult; Angiomyoma; Female; Humans; Urination Disorders; Vaginal Neoplasms
PubMed: 9751375
DOI: 10.1097/00005392-199810000-00064 -
Ear, Nose, & Throat Journal Dec 2020
Topics: Angiomyoma; Epistaxis; Humans; Male; Medical Illustration; Middle Aged; Nasal Cavity; Nasal Obstruction; Paranasal Sinus Neoplasms
PubMed: 31272210
DOI: 10.1177/0145561319858913 -
The Journal of Laryngology and Otology Dec 2003Angiomyoma is a common soft tissue tumour of the head and neck that sometimes presents to the otolaryngologist; however, it seldom occurs in the major salivary glands.... (Review)
Review
Angiomyoma is a common soft tissue tumour of the head and neck that sometimes presents to the otolaryngologist; however, it seldom occurs in the major salivary glands. We present a case of angiomyoma arising in the submandibular gland, a tumour not described previously in the English literature.
Topics: Adult; Angiomyoma; Female; Humans; Submandibular Gland; Submandibular Gland Neoplasms
PubMed: 14738618
DOI: 10.1258/002221503322683966 -
Indian Journal of Dermatology,... 2017
Topics: Adult; Angiomyoma; Female; Humans; Nails; Skin Neoplasms
PubMed: 27364928
DOI: 10.4103/0378-6323.185045