Medicine:Epithelial-myoepithelial carcinoma of the lung

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Epithelial-myoepithelial carcinoma of the lung
Other namesEMECL Adenomyoepithelioma,[1] Myoepithelioma, Epithelial-myoepithelial tumor, Epimyoepithelial carcinoma, Malignant mixed tumor containing epithelial and myoepithelial cells.[2]
SpecialtyOncology

Epithelial-myoepithelial carcinoma of the lung is a very rare histologic form of malignant epithelial neoplasm ("carcinoma") arising from lung tissue.[2]

Genetics

The epithelial component in EMECL's typically strongly express cytokeratins, but are negative for actin and S-100 protein, while the myoepithelial component stains strongly for actin and S-100 protein, and only focally weakly for cytokeratins.[3]

Diagnosis

Microscopically, EMECL features bi-layered glandular or ductular structures consisting of inner cuboidal cells and outer multipolar cells.[4]

The histologic appearance of these tumors varied, but all shared the common feature of a biphasic proliferation of epithelial (strong cytokeratin-positive; actin and S-100-negative) and myoepithelial (strong actin and S-100 and focal weak cytokeratin-positive) cells with formation of bilayered ductlike structures. The focal resemblance to other salivary gland-type tumors may cause diagnostic difficulties, particularly in small endobronchial biopsies. Although little is known about their biologic potential due to limited follow-up data, these tumors when in the lung clearly have the capacity to infiltrate and metastasize and therefore should be designated as epithelial-myoepithelial carcinoma. At present, it appears that treatment by complete surgical resection with negative margins alone is appropriate and adequate.[3]

Classification

Lung cancer is an extremely heterogeneous family of malignant neoplasms,[5] with well over 50 different histological variants recognized under the 4th revision of the World Health Organization (WHO) typing system ("WHO-2004"),[2] currently the most widely used lung cancer classification scheme. Because these variants have differing genetic, biological, and clinical properties, including response to treatment, correct classification of lung cancer cases are necessary to assure that lung cancer patients receive optimum management.[2][6][7]

The WHO-2004 scheme groups lung carcinomas into 8 major types:[2]

  • Squamous cell carcinoma
  • Small cell carcinoma
  • Adenocarcinoma
  • Large cell carcinoma
  • Adenosquamous carcinoma
  • Sarcomatoid carcinoma
  • Carcinoid tumor
  • Salivary gland-like carcinoma

EMECL is considered a subtype of salivary gland-like carcinoma, tumors so named because their histological appearance and characteristics closely resemble malignant neoplasms arising in the major and minor salivary glands.[citation needed]

Staging

EMECL is staged in the same manner as other non-small cell lung carcinomas, based on the TNM (Tumor-Node-Metastasis) staging system.[8]

Treatment

Complete radical surgical resection is the treatment of choice for EMECL, and in most cases, results in long-term survival or cure.[9][10]

Prognosis

The prognosis of EMECL is relatively good, and considerably better than most other forms of NSCLC. The skull and dura are possible sites for metastasis from pulmonary EMC. The MIB-1 index is a predictive marker of malignant potential.[citation needed]

Incidence

EMECL is extremely rare, with only a handful of cases reported in the literature.[11]

In the lung, two salivary gland-like carcinomas, mucoepidermoid carcinoma and adenoid cystic carcinoma, while extremely uncommon, occur far more often than does EMECL.[2][12]

References

  1. ↑ "Adenomyoepithelioma of the lung". The American Journal of Surgical Pathology 19 (8): 956–62. August 1995. doi:10.1097/00000478-199508000-00012. PMID 7611543. 
  2. ↑ 2.0 2.1 2.2 2.3 2.4 2.5 Travis, William D; Brambilla, Elisabeth; Muller-Hermelink, H Konrad et al., eds (2004). Pathology and Genetics of Tumours of the Lung, Pleura, Thymus and Heart. World Health Organization Classification of Tumours. Lyon: IARC Press. ISBN 92-832-2418-3. http://www.iarc.fr/en/publications/pdfs-online/pat-gen/bb10/bb10-cover.pdf. Retrieved 27 March 2010. 
  3. ↑ 3.0 3.1 "Pulmonary epithelial-myoepithelial carcinoma: a clinicopathologic and immunohistochemical study of 5 cases". Human Pathology 40 (3): 366–73. March 2009. doi:10.1016/j.humpath.2008.08.009. PMID 18973918. 
  4. ↑ Okudela K et al. (February 2010). "A case of epithelial-myoepithelial carcinoma of the bronchus - a review of reported cases and a comparison with other salivary gland-type carcinomas of the bronchus". Pathol. Res. Pract. 206 (2): 121–9. doi:10.1016/j.prp.2009.03.003. PMID 19369010. 
  5. ↑ "Lung cancer heterogeneity: a blinded and randomized study of 100 consecutive cases". Human Pathology 16 (6): 569–79. June 1985. doi:10.1016/S0046-8177(85)80106-4. PMID 2987102. 
  6. ↑ "Histotype in non-small cell lung cancer therapy and staging: The emerging role of an old and underrated factor". Curr Respir Med Rev 3: 69–77. 2007. doi:10.2174/157339807779941820. 
  7. ↑ Vincent MD (August 2009). "Optimizing the management of advanced non-small-cell lung cancer: a personal view". Curr Oncol 16 (4): 9–21. doi:10.3747/co.v16i4.465. PMID 19672420. 
  8. ↑ "The revised TNM staging system for lung cancer". Annals of Thoracic and Cardiovascular Surgery 15 (1): 4–9. February 2009. PMID 19262443. 
  9. ↑ Muro M et al. (March 2010). "肺に発生した上皮-筋上皮癌" (in ja). Kyobu Geka 63 (3): 220–3. PMID 20214352. http://www.pieronline.jp/openurl?issn=0021-5252&volume=63&issue=3&spage=220. 
  10. ↑ "Skull metastasis as initial manifestation of pulmonary epithelial-myoepithelial carcinoma: a case report of an unusual case". Case Reports in Oncological Medicine 2011: 610383. 2011. doi:10.1155/2011/610383. PMID 22629483. 
  11. ↑ "Epithelial-myoepithelial carcinoma of the lung. A case report and review of the literature". Archives of Pathology & Laboratory Medicine 127 (4): e177–80. April 2003. doi:10.5858/2003-127-e177-ECOTL. PMID 12683896. 
  12. ↑ "Lung cancer". Cancer 75 (1 Suppl): 191–202. January 1995. doi:10.1002/1097-0142(19950101)75:1+<191::AID-CNCR2820751307>3.0.CO;2-Y. PMID 8000996. 

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