- Ossifying fibromyxoid tumour
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Ossifying fibromyxoid tumour Classification and external resources ICD-O: 8842/0 An ossifying fibromyxoid tumour is a type of myxoma.
It presents in the extremities more frequently than the trunk.[1]
It is derived from mesenchyme.[2]
Appearance in the head and neck is rare, but has been reported.[3]
Their malignancy has been characterized as "intermediate".[4]
References
- ^ Makhson AN, Bulycheva IV, Kuz'min IV, Denisov AK, Groshev IA (2006). "[Ossifying fibromyxoid tumor]" (in Russian). Arkh. Patol. 68 (2): 41–4. PMID 16752509.
- ^ Seykora JT, Kutcher C, van de Rijn M, Dzubow L, Junkins-Hopkins J, Ioffreda M (2006). "Ossifying fibromyxoid tumor of soft parts presenting as a scalp cyst". J. Cutan. Pathol. 33 (8): 569–72. doi:10.1111/j.1600-0560.2006.00444.x. PMID 16919031. http://www.blackwell-synergy.com/openurl?genre=article&sid=nlm:pubmed&issn=0303-6987&date=2006&volume=33&issue=8&spage=569.
- ^ Mollaoglu N, Tokman B, Kahraman S, Cetiner S, Yucetas S, Uluoglu O (2006). "An unusual presentation of ossifying fibromyxoid tumor of the mandible: a case report". J Clin Pediatr Dent 31 (2): 136–8. PMID 17315811.
- ^ Folpe AL, Weiss SW (2003). "Ossifying fibromyxoid tumor of soft parts: a clinicopathologic study of 70 cases with emphasis on atypical and malignant variants". Am. J. Surg. Pathol. 27 (4): 421–31. doi:10.1097/00000478-200304000-00001. PMID 12657926. http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?issn=0147-5185&volume=27&issue=4&spage=421.
Connective/soft tissue tumors and sarcomas (ICD-O 8800–9059) (C45–C49/D17–D21, 171/214–215) Not otherwise specified (8800–8809) Connective tissue neoplasm Fibromatous (8810–8839)Fibroma/fibromatosis: Aggressive infantile fibromatosis · Aponeurotic fibroma · Collagenous fibroma · Diffuse infantile fibromatosis · Familial myxovascular fibromas · Fibroma of tendon sheath · Fibromatosis colli · Infantile digital fibromatosis · Juvenile hyaline fibromatosis · Plantar fibromatosis · Pleomorphic fibroma · Oral submucous fibrosisHistiocytoma/histiocytic sarcoma: Benign fibrous histiocytoma · Malignant fibrous histiocytoma · Atypical fibroxanthomaSolitary fibrous tumorMyxomatous (8840–8849)Myxoma/myxosarcoma (Cutaneous myxoma, Superficial acral fibromyxoma) · Angiomyxoma · Ossifying fibromyxoid tumourFibroepithelial (9000–9039)Synovial-like (9040–9049)Lipomatous (8850–8889) Chondroid lipoma · Intradermal spindle cell lipoma · Pleomorphic lipoma · Benign lipoblastomatosis · Spindle cell lipoma · HibernomaMyomatous (8890–8929) general: Myoma/myosarcomaskeletal muscle: Rhabdomyoma/rhabdomyosarcoma: Embryonal rhabdomyosarcoma (Sarcoma botryoides) · Alveolar rhabdomyosarcomaLeiomyoma · Angioleiomyoma · Angiolipoleiomyoma · Genital leiomyoma · Leiomyosarcoma · Multiple cutaneous and uterine leiomyomatosis syndrome · Multiple cutaneous leiomyoma · Neural fibrolipoma · Solitary cutaneous leiomyomaComplex mixed and stromal (8930–8999) Adenomyoma · Pleomorphic adenoma · Mixed Müllerian tumor · Mesoblastic nephroma · Wilms' tumor · Rhabdoid tumour · Clear-cell sarcoma of the kidney · Hepatoblastoma · Pancreatoblastoma · CarcinosarcomaMesothelial (9050–9059) see also Template:Connective tissue
Embryology of bones, joints, and muscles (GA 2.80, TE E5.0-2) Ossification Lower limbHeadcranium: Ossification of occipital bone · Ossification of frontal bone · Ossification of temporal bone · Ossification of sphenoid · Ossification of ethmoid
facial bones: Ossification of vomer (Sutura vomerina · Foramen vomerinum · Meatus vomerinus · Fissura vomerina) · Ossification of maxilla · Ossification of mandibleOtherOther M: JNT
anat(h/c, u, t, l)/phys
noco(arth/defr/back/soft)/cong, sysi/epon, injr
proc, drug(M01C, M4)
Categories:- Connective and soft tissue neoplasms
- Tissues
- Disease stubs
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