« Previous
Next »
Diagnostic Histopathology
Volume 14, Issue 11
, Pages 527-537
, November 2008
Pleomorphic sarcomas: subclassification, myogenic differentiation and prognosis
References
- In: Fletcher CDM, Unni KK, Mertens F editor. World Health Organization classification of tumours. Pathology and genetics of tumors of soft tissue and bone. Lyon: IARC Press; 2002;
- In: Weiss SW, Goldblum JR editor. Enzinger and Weiss’s soft tissue tumors. 5th edn.. St Louis: Mosby-Elsevier; 2008;
- . Pleomorphic malignant fibrous histiocytoma: fact or fiction? A critical reappraisal based on 159 tumors diagnosed as pleomorphic sarcoma. Am J Surg Pathol. 1992;16:213–228
- . The evolving classification of soft tissue tumours: an update based on the new WHO classification. Histopathology. 2006;48:3–12
- . Classification of pleomorphic sarcomas: where are we now?. Histopathology. 2006;48:51–62
- . Malignant fibrous xanthomas. Cancer. 1964;17:1445–1455
- . Fibroxanthosarcoma of the soft tissues: a type of malignant fibrous histiocytoma. Cancer. 1972;29:961–976
- . Malignant fibrous histiocytoma: an analysis of 200 cases. Cancer. 1978;41:2250–2266
- . Malignant fibrous histiocytoma: a reaffirmation. Am J Surg Pathol. 1982;6:773–784
- . Microarray analysis of sarcomas. Adv Anat Pathol. 2006;13:166–173
- Gene expression analysis of soft tissue sarcomas: characterization and reclassification of malignant fibrous histiocytoma. Mod Pathol. 2007;20:749–759
- Inflammatory malignant fibrous histiocytomas and dedifferentiated liposarcomas: histologic review, genomic profile, and MDM2 and CDK4 status favour a single entity. J Pathol. 2004;203:822–830
- Most malignant fibrous histiocytomas developed in the retroperitoneum are dedifferentiated liposarcomas: a review of 25 cases initially diagnosed as malignant fibrous histiocytoma. Mod Pathol. 2003;16:256–262
- . Evaluation of biological potential of smooth muscle tumours. Histopathology. 2006;48:97–105
- . Inflammatory leiomyosarcoma: a morphological subgroup within the heterogeneous family of so- called inflammatory malignant fibrous histiocytoma. Histopathology. 1995;27:525–532
- . Leiomyosarcoma with prominent osteoclast-like giant cells. Analysis of eight cases closely mimicking the so-called giant cell variant of malignant fibrous histiocytoma. Am J Surg Pathol. 1994;18:258–265
- A gene expression signature associated with metastatic outcome in human leiomyosarcomas. Cancer Res. 2004;64:7201–7204
- Gene expression analysis of human soft tissue leiomyosarcomas. Hum Pathol. 2003;34:549–558
- Proteomic signatures corresponding to histological classification and grading of soft-tissue sarcomas. Proteomics. 2006;6:4402–4409
- Pérot G, Derré J, Coindre JM, et al. Myocardin amplification and overexpression induce a strong smooth muscle differentiation in retroperitoneal leiomyosarcomas, in press.
- . Pleomorphic rhabdomyosarcoma in adults: a clinicopathologic study of 38 cases with emphasis on morphologic variants and recent skeletal muscle-specific markers. Mod Pathol. 2001;14:595–603
- Adult rhabdomyosarcoma. Outcome following multimodality treatment. Cancer. 2002;95:377–388
- . Dedifferentiated liposarcoma. A clinicopathological analysis of 155 cases with a proposal for an expanded definition of dedifferentiation. Am J Surg Pathol. 1997;21:271–281
- . Dedifferentiated liposarcoma. Clinicopathologic analysis of 32 cases suggesting a better prognostic subgroup among pleomorphic sarcomas. Am J Surg Pathol. 1994;18:1213–1223
- . Distant metastasis in retroperitoneal dedifferentiated liposarcoma is rare and rapidly fatal: a clinicopathological study with emphasis on the low-grade myxofibrosarcoma-like pattern as an early sign of dedifferentiation. Mod Pathol. 2005;18:976–984
- Dedifferentiated liposarcomas with divergent myosarcomatous differentiation developed in the internal trunk. A study of 27 cases and comparison to conventional dedifferentiated liposarcomas and leiomyosarcomas. Am J Surg Pathol. 2007;31:1557–1566
- MDM2 and CDK4 immunostainings are useful adjuncts in diagnosing well-differentiated and dedifferentiated liposarcoma subtypes: A comparative analysis of 559 soft tissue neoplasms with genetic data. Am J Surg Pathol. 2005;29:1340–1347
- Detection of MDM2-CDK4 amplification by fluorescence in situ hybridization (FISH) in 200 paraffin-embedded tumor samples: utility in the differential diagnostic approach of adipocytic lesions and comparison with immunohistochemistry and real time PCR. Am J Surg Pathol. 2007;31:1476–1489
- . Updates on the cytogenetics and molecular genetics of bone and soft tissue tumors: liposarcoma. Cancer Genet Cytogenet. 2004;155:1–24
- ASK1 (MAP3K5) as a potential therapeutic target in malignant fibrous histiocytomas with 12q14- q15 and 6q23 amplifications. Genes Chromosomes Cancer. 2004;40:32–37
- JUN oncogene amplification and overexpression block adipocytic differentiation in highly aggressive sarcomas. Cancer Cell. 2007;11:361–374
- Pleomorphic liposarcoma: clinicopathologic, immunohistochemical, and follow-up analysis of 63 cases. A study from the French Federation of Cancer Centers Sarcoma Group. Am J Surg Pathol. 2002;26:601–616
- . Plemorphic liposarcoma. Clinicopathologic analysis of 57 cases. Am J Surg Pathol. 2004;28:1257–1267
- . Primary liposarcoma of the skin: a rare neoplasm with unusual high grade features. Am J Dermatopathol. 1998;20:332–338
- . Epithelioid variant of pleomorphic liposarcoma: a study of 12 cases of a distinctive variant of high-grade liposarcoma. Mod Pathol. 1999;12:722–728
- . Myxofibrosarcoma. A malignant soft tissue tumor of fibroblastic-histiocytic origin. A clinicopathologic and prognostic study of 110 cases using multivariate analysis. Acta Pathol Microbiol Immunol Scand. 1983;282(Suppl):1–40
- Myxofibrosarcoma: clinicopathologic analysis of 75 cases with emphasis on the low grade variant. Am J Surg Pathol. 1996;20:391–405
- . Low-grade myxofibrosarcoma: a clinicopathologic analysis of 49 cases treated at a single institution with simultaneous assessment of the efficacy of 3-tier and 4-tier grading systems. Hum Pathol. 2004;35:612–621
- 39a Prognostic factors of myxofibrosarcomas: implications of margin status, tumor necrosis, and mitotic rate on survival. J Surg Oncol. 2006;93:294–30339b. Epithelioid variant of myxofibrosarcoma: expanding the clinicomorphologic spectrum of myxofibrosarcoma in a series of 17 cases. Am J Surg Pathol. 2007;31:99–105
- . Myofibroblastic differentiation in malignant fibrous histiocytoma (pleomorphic myofibrosarcoma): a clinicopathological study. Histopathology. 2001;38:499–509
- . Myofibrosarcoma. Virchows Arch. 2004;445:215–223
- . Pleomorphic hyalinizing angiectatic tumor of soft parts. A low-grade neoplasm resembling neurilemoma. Am J Surg Pathol. 1996;20:21–29
- . Pleomorphic hyalinizing angiectatic tumor. Analysis of 41 cases supportring evolution from a distinctive precursor lesion. Am J Surg Pathol. 2004;28:1417–1425
- . Inflammatory myxohyaline tumor of distal extremities with virocyte or Reed-Sternberg-like cells: a distinctive lesion with features simulating inflammatory conditions, Hodgkin’s disease, and various sarcomas. Mod Pathol. 1998;11:384–391
- . Acral myxoinflammatory fibroblastic sarcoma: a low-grade tumor of the hands and feet. Am J Surg Pathol. 1998;22:911–924
- Clinicopathologic re- evaluation of 100 malignant fibrous histiocytomas: prognostic relevance of subclassification. J Clin Oncol. 2001;19:3045–3050
- Myoid differentiation and prognosis in adult pleomorphic sarcomas of the extremity: an analysis of 92 cases. Cancer. 2003;98:805–813
PII: S1756-2317(08)00150-3
doi: 10.1016/j.mpdhp.2008.08.002
« Previous
Next »
Diagnostic Histopathology
Volume 14, Issue 11
, Pages 527-537
, November 2008

