| Mixed Müllerian tumor | 
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| Classification and external resources | 
| ICD-O: | 8950 | 
A malignant mixed Müllerian tumor, also known as malignant mixed mesodermal tumor, MMMT and carcinosarcoma, is a malignant neoplasm found in the uterus, the ovaries, the fallopian tubes and other parts of the body that contains both carcinomatous (epithelial tissue) and sarcomatous (connective tissue) components. It is divided into two types, homologous (in which the sarcomatous component is made of tissues found in the uterus such as endometrial, fibrous and/or smooth muscle tissues) and a heterologous type (made up of tissues not found in the uterus, such as cartilage, skeletal muscle and/or bone). MMMT account for between two and five percent of all tumors derived from the body of the uterus, and are found predominantly in postmenopausal women with an average age of 66 years. Risk factors are similar to those of adenocarcinomas and include obesity, exogenous estrogen therapies, and nulliparity. Less well-understood but potential risk factors include tamoxifen therapy and pelvic irradiation.[1]
Contents
- 1 Naming and classification
- 2 Morphology
- 3 Prognosis
- 4 References
 
Naming and classification
There is debate over the naming of MMMT; the term carcinosarcoma was formerly used to describe lesions with homologous tumors, and "malignant mixed Müllerian tumor" or "mixed mesodermal tumor" was used to describe heterologous tumors. While "carcinosarcoma" now considered standard, "malignant mixed Müllerian tumor" has a lengthy history within gynecological literature and is expected to continue to be used. The naming issue to a certain extent reflects histological characteristics and development of the tumors, in which the different types of tissues are believed to either develop separately and join into a single mass (the "collision" theory), that an adenocarcinoma stimulates the stroma to create a tumor (the "composition" theory), or that the tumor is the result of a stem cell that differentiates into different cell types (the "combination" theory).[1] "Collision" tumors are normally easily recognized and not considered true MMMTs; the "combination" theory is most widely held, and is due to evidence that the tumors develop from a single line of cells, developing in a fashion similar to the fundus of the uterus from the Müllerian duct - first from a stem cell into a population of cells, that then differentiates into epithelial and stromal components.[1][2]
There is evidence that some tumors are better explained by the composition theory, due to the aggressive nature of the epithelial cells involved which tend to metastasize much more readily than the sarcomal component. The behavior of MMMT overall is more related to the type and grade of the epithelium than the sarcoma, which suggests the sarcomal portion is an atypical "bystander" than primary driver of the tumor. Despite this, when purely endometrial tumors are compared to MMMTs, the MMMT tumor tends to have a worse prognosis.[1]
Morphology
Carcinosarcoma of the uterus
 
 
 
In gross appearance, MMMTs are fleshier than adenocarcinomas, may be bulky and polypoid, and sometimes protrude through the cervical os. On histology, the tumors consist of adenocarcinoma (endometrioid, serous or clear cell) mixed with the malignant mesenchymal (sarcoma) elements; alternatively, the tumor may contain two distinct and separate epithelial and mesenchymal components. Sarcomatous components may also mimic extrauterine tissues (e.g., striated muscle, cartilage, adipose tissue, and bone). Metastases usually contain only epithelial components.
Prognosis
Outcome of MMMTs is determined primarily by depth of invasion and stage. As with endometrial carcinomas, the prognosis is influenced by the grade and type of the adenocarcinoma, being poorest with serous differentiation. MMMTs are highly malignant; a stage I tumor has an expected five-year survival rate of 50%, while the overall five-year survival rate is less than 20%.[1]
Staging of Uterine MMMTs is as follows:[3]
- Stage I. Carcinoma is confined to the corpus uteri itself.
- Stage II. Carcinoma involves the corpus and the cervix.
- Stage III. Carcinoma extends outside the uterus but not outside the lesser pelvis.
- Stage IV. Carcinoma extends outside the true pelvis or involves the mucosa of the bladder or the rectum.
References
- ^ a b c d e Siegal GP; Chhieng DC (2005). Updates in diagnostic pathology. Berlin: Springer. pp. 12–14. ISBN 0-387-25357-2. 
- ^ Abeln, E. C. A.; Smit, V. T. H. B. M.; Wessels, J. W.; De Leeuw, W. J. F.; Cornelisse, C. J.; Fleuren, G. J. (1997). "Molecular genetic evidence for the conversion hypothesis of the origin of malignant mixed Müllerian tumours". Journal of Pathology 183 (4): 424–431. doi:10.1002/(SICI)1096-9896(199712)183:4<424::AID-PATH949>3.0.CO;2-L. PMID 9496259.  edit
- ^ Jon Aster MD; Vinay Kumar MBBS MD FRCPath; Abul K. Abbas MBBS; Nelson Fausto MD (2009). Robbins & Cotran Pathologic Basis of Disease. Philadelphia: Saunders. ISBN 1-4160-3121-9. 
 
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| Connective/soft tissue tumors and sarcomas (ICD-O 8800–9059) (C45–C49/D17–D21, 171/214–215) |  
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| Not otherwise specified | 
Soft-tissue sarcomaDesmoplastic small-round-cell tumor |  
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| Connective tissue neoplasm | 
| Fibromatous | 
| Fibroma/fibrosarcoma: | 
Dermatofibrosarcoma protuberansDesmoplastic fibroma |  
|  |  
| Fibroma/fibromatosis: | 
Aggressive infantile fibromatosisAponeurotic fibromaCollagenous fibromaDiffuse infantile fibromatosisFamilial myxovascular fibromasFibroma of tendon sheathFibromatosis colliInfantile digital fibromatosisJuvenile hyaline fibromatosisPlantar fibromatosisPleomorphic fibromaOral submucous fibrosis |  
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| Histiocytoma/histiocytic sarcoma: | 
Benign fibrous histiocytomaMalignant fibrous histiocytomaAtypical fibroxanthomaSolitary fibrous tumor |  |  
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| Myxomatous | 
Myxoma/myxosarcoma
Cutaneous myxomaSuperficial acral fibromyxomaAngiomyxomaOssifying fibromyxoid tumour |  
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| Fibroepithelial | 
Brenner tumourFibroadenomaPhyllodes tumor |  
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| Synovial-like | 
Synovial sarcomaClear-cell sarcoma |  |  
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| Lipomatous | 
Lipoma/liposarcoma
MyelolipomaMyxoid liposarcomaPEComa
 
Chondroid lipomaIntradermal spindle cell lipomaPleomorphic lipomaLipoblastomatosisSpindle cell lipomaHibernoma |  
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| Myomatous | 
| general: |  |  
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| smooth muscle: |  |  
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| skeletal muscle: | 
Rhabdomyoma/rhabdomyosarcoma: Embryonal rhabdomyosarcoma
Alveolar rhabdomyosarcoma |  
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| 
LeiomyomaAngioleiomyomaAngiolipoleiomyomaGenital leiomyomaLeiomyosarcomaMultiple cutaneous and uterine leiomyomatosis syndromeMultiple cutaneous leiomyomaNeural fibrolipomaSolitary cutaneous leiomyomaSTUMP |  |  
|  |  
| Complex mixed and stromal | 
AdenomyomaPleomorphic adenomaMixed Müllerian tumorMesoblastic nephromaWilms' tumorMalignant rhabdoid tumourClear-cell sarcoma of the kidneyHepatoblastomaPancreatoblastomaCarcinosarcoma |  
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| Mesothelial | 
MesotheliomaAdenomatoid tumor |  
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| Description | 
Anatomy
headneckarmschest and backdiaphragmabdomengenital arealegsMuscle tissuePhysiologyDevelopment |  
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| Disease | 
MyopathySoft tissueConnective tissueCongenital
abdomenmuscular dystrophyNeoplasms and cancerInjurySymptoms and signs
 |  
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| Treatment | 
ProceduresDrugs
anti-inflammatorymuscle relaxants |  |  | 
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| Tumors: female urogenital neoplasia (C51–C58/D25–D28, 179–184/218–221) |  
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| Adnexa | 
| Ovaries | 
| Glandular and epithelial/ 
 surface epithelial-stromal tumor
 | 
| CMS: | 
Ovarian serous cystadenomaMucinous cystadenomaCystadenocarcinoma
Papillary serous cystadenocarcinomaKrukenberg tumor |  
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Endometrioid tumorClear-cell ovarian carcinomaBrenner tumour |  |  
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| Sex cord-gonadal stromal | 
Leydig cell tumourSertoli cell tumourSertoli-Leydig cell tumourThecomaGranulosa cell tumourLuteomaSex cord tumour with annular tubulesSteroid cell tumor (NOS) |  
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| Germ cell | 
DysgerminomaNongerminomatous
Embryonal carcinomaEndodermal sinus tumorGonadoblastomaTeratoma/Struma ovariiChoriocarcinoma |  
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| Fibroma |  |  |  
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| Fallopian tube |  |  |  
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| Uterus | 
| Myometrium | 
Uterine fibroids/leiomyomaLeiomyosarcomaAdenomyoma |  
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| Endometrium | 
Endometrioid tumorUterine papillary serous carcinomaClear cell carcinomaEndometrial intraepithelial neoplasia |  
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| Cervix | 
Cervical intraepithelial neoplasiaSCCGlassy cell carcinomaVilloglandular adenocarcinoma |  
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| Placenta | 
ChoriocarcinomaGestational trophoblastic disease |  
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| General | 
Uterine sarcomaMixed Müllerian tumor |  |  
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| Vagina | 
SCCBotryoid rhabdomyosarcomaClear cell adenocarcinoma of the vaginaVaginal intraepithelial neoplasia |  
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| Vulva | 
SCCMelanomaPapillary hidradenomaExtramammary Paget's diseaseVulvar intraepithelial neoplasia |  
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Index of the female reproductive system
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| Description | 
AnatomyPhysiology
Development |  
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| Disease | 
CongenitalNeoplasms and cancerOtherSymptoms and signs
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| Treatment | 
ProceduresDrugs
infectionestrogensprogestogensAssisted reproductionBirth control |  |  |