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词条 Ectomesenchymal chondromyxoid tumor
释义

  1. Controversies about origin

  2. Signs and Symptoms

  3. Management

  4. Pathology findings

      Macroscopic    Microscopic Pathology    Immunohistochemistry    Ancillary Studies    Differential diagnoses  

  5. Epidemiology

  6. References

  7. Further reading

Ectomesenchymal chondromyxoid tumor (ECT) is a benign intraoral tumor with presumed origin from undifferentiated (ecto)mesenchymal cells.[1] There are some who think it is a myoepithelial tumor type.[2]

Controversies about origin

  • Derived from ectomesenchymal cells migrating from neural crest (there is immunophenotypic support for this theory).[1]
  • Equivalent to soft tissue myoepithelioma. There is morphologic and immunohisthochemical support for this theory, with some authors advocating interchangeable terms.[3][4]

Signs and Symptoms

Patients present with a painless, slow-growing mass usually within the tongue (most commonly the anterior dorsal tongue). There is an intact surface epithelium.[1][5][6]

Management

  • Surgical excision is the treatment of choice, with recurrences only when there is incomplete excision.[1]

Pathology findings

Macroscopic

  • Submucosal circumscribed but not encapsulated nodular mass, often with entrapped muscle bundles at the edge. It may have a gelatinous appearance. Most tumors are small, up to 2 cm (given the confines of the tongue, a larger mass would cause significant clinical problems).[1][5][6]

Microscopic Pathology

  • Submucosal unencapsulated but well-delineated or circumscribed nodule, often separated from the periphery and internally by fibrous connective tissue bands. The cells are arranged in cords, nests, and net-like sheets. The cells may extend into and entrap soft tissue structures including skeletal muscle and nerve bundles.[5][6]
  • The tumor is made up of small round, oval, spindle, or stellate cells that have a very monotonous appearance. There are small dark nuclei with variably amounts of light to basophilic cytoplasm.[1][5][7]
  • Nuclear pleomorphism, multinucleation, and mitotic figures are usually not seen. Atypical mitoses and necrosis is absent.[6]
  • There is a background stroma composed of chondromyxoid to myxoid material. Sometimes large cells are seen in chondroid or cartilaginous areas. Swirling formations give the appearance of neural tissue.[7]
  • Importantly, there is an absence of glands or myoepithelial components.[1][3]

Immunohistochemistry

  • Positive: Glial fibrillary acidic protein (GFAP), pancytokeratin, and S100 protein. Smooth muscle actin may be positive in about 50% of cases.[1][6]
  • Negative: Epithelial membrane antigen, desmin, p63 and calponin.[5][7]

Ancillary Studies

  • Alcian blue will give a blue staining to the stromal matrix material.
  • Mucicarmine will also highlight the stromal matrix (pink).

Differential diagnoses

The tumor is quite unique, but other tumors are considered in the differential diagnosis histologically. They included pleomorphic adenoma, myoepithelioma, myxoid neurofibroma, neurothekeoma (nerve sheath myxoma), chondroid choristoma, extraskeletal myxoid chondrosarcoma, focal oral mucinosis, and an ossifying fibromyxoid tumor of soft parts.[1]

Epidemiology

Exceedingly rare, this tumor develops in a wide age range, although often in young patients without a sex predilection. The vast majority develop within the anterior dorsal tongue,[1] with palate and base of tongue rarely affected.[8]

References

1. ^1 2 3 4 5 6 7 8 9 {{cite journal |vauthors=Smith BC, Ellis GL, Meis-Kindblom JM, Williams SB |date=May 1995 |title=Ectomesenchymal chondromyxoid tumor of the anterior tongue. Nineteen cases of a new clinicopathologic entity |journal=Am J Surg Pathol |pmid=7726361 |volume=19 |issue=5 |pages=519–30 |doi=10.1097/00000478-199505000-00003}}
2. ^{{cite journal |vauthors=Woo VL, Angiero F, Fantasia JE |date=May 2005 |title=Myoepithelioma of the tongue |journal=Oral Surg Oral Med Oral Pathol Oral Radiol Endod |pmid=15829881 |doi=10.1016/j.tripleo.2004.12.016 |volume=99 |issue=5 |pages=581–9}}
3. ^1 {{cite journal |vauthors=Goveas N, Ethunandan M, Cowlishaw D, Flood TR |date=November 2006 |title=Ectomesenchymal chondromyxoid tumour of the tongue: Unlikely to originate from myoepithelial cells |journal=Oral Oncol |pmid=17011812 |doi=10.1016/j.oraloncology.2006.06.004 |volume=42 |issue=10 |pages=1026–8}}
4. ^{{cite journal |vauthors=Seo SH, Shin DH, Kang HJ, Choi KU, Kim JY, Park do Y, Lee CH, Sol MY, Lee JC |date=October 2010 |title=Reticulated myxoid tumor of the tongue: 2 cases supporting an expanded clinical and immunophenotypic spectrum of ectomesenchymal chondromyxoid tumor of the tongue |journal=Am J Dermatopathol |pmid=20661118 |doi=10.1097/DAD.0b013e3181d7d3bf |volume=32 |issue=7 |pages=660–4}}
5. ^1 2 3 4 {{cite journal |vauthors=Kannan R, Damm DD, White DK, Marsh W, Allen CM |date=October 1996 |title=Ectomesenchymal chondromyxoid tumor of the anterior tongue: a report of three cases |journal=Oral Surg Oral Med Oral Pathol Oral Radiol Endod |pmid=8899780 |volume=82 |issue=4 |pages=417–22}}
6. ^1 2 3 4 {{cite journal |vauthors=Pires FR, Abrahão AC, Cabral MG, Azevedo RS, Horta MC, Martins CR, de Almeida OP, Chen SY |date=December 2009 |title=Clinical, histological and immunohistochemical features of ectomesenchymal chondromyxoid tumor |journal=Oral Surg Oral Med Oral Pathol Oral Radiol Endod |pmid=19800267 |doi=10.1016/j.tripleo.2009.07.007 |volume=108 |issue=6 |pages=914–9}}
7. ^1 2 {{cite journal |author=Angiero F |date=November 2010 |title=Ectomesenchymal chondromyxoid tumour of the tongue. A review of histological and immunohistochemical features |journal=Anticancer Res |pmid=21115924 |volume=30 |issue=11 |pages=4685–9}}
8. ^{{cite journal |vauthors=Nigam S, Dhingra KK, Gulati A |date=February 2006 |title=Ectomesenchymal chondromyxoid tumor of the hard palate--a case report |journal=J Oral Pathol Med |pmid=16430745 |doi=10.1111/j.1600-0714.2006.00368.x |volume=35 |issue=2 |pages=126–8}}

Further reading

  • {{citation|title=Diagnostic Pathology: Head and Neck, 2e|last=Thompson|first= Lester D.R.|publisher=Elsevier|year=2016|isbn=978-0323392556}}
{{Oral pathology}}

1 : Salivary gland neoplasia
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