You have 1 free disease view remaining today. Register for more view, it is 100% free โ
mucoepidermoid carcinoma
Description
Mucoepidermoid carcinoma (MEC) is a type of cancer that affects the salivary glands, as well as other organs such as the bronchi, lacrimal sac, and thyroid gland [2]. It is characterized by the presence of three distinct cell types: mucus-producing cells, epidermoid (squamous-like) cells, and intermediate cells that share features of the other two cell types [12].
Mucoepidermoid carcinoma can range from low-grade to high-grade, with the latter being more aggressive and likely to spread to other body parts [12]. The classic description of MEC is composed of these three cell types: epidermoid, intermediate, and mucin-producing cells [13].
This type of cancer is relatively rare, but it is the most common malignant salivary gland tumor, accounting for 10-15% of all salivary gland tumors and one-third of all salivary gland malignancies [14]. Mucoepidermoid carcinoma can arise from reserve cells of excretory ducts that are pluripotent in nature.
The symptoms of mucoepidermoid carcinoma may include facial pain and tenderness, facial paralysis, jaw spasms, and other signs depending on the location and severity of the tumor. It is essential to note that not all cases of MEC cause noticeable symptoms [11].
Mucoepidermoid carcinomas can be mistaken for other types of cancer, such as squamous cell carcinoma, especially in higher-grade tumors [10]. The diagnosis of MEC typically involves a combination of clinical evaluation, imaging studies, and histopathological examination.
References: [1] Context result 2 [2] Context result 2 [3] Context result 2 [4] Context result 4 [5] Context result 5 [6] Context result 6 [7] Context result 7 [8] Context result 8 [9] Context result 9 [10] Context result 10 [11] Context result 11 [12] Context result 12 [13] Context result 13 [14] Context result 14
Additional Characteristics
- facial paralysis
- thyroid gland
- Mucoepidermoid carcinoma
- salivary glands
- squamous cell carcinoma
- bronchi
- lacrimal sac
- mucus-producing cells
- epidermoid (squamous-like) cells
- intermediate cells
- low-grade
- high-grade
- facial pain and tenderness
- jaw spasms
Signs and Symptoms
Diagnostic Tests
Mucoepidermoid carcinoma, a type of salivary gland cancer, can be diagnosed using various tests and examinations. Here are some of the diagnostic tests that may be used to diagnose mucoepidermoid carcinoma:
- Biopsy: A biopsy is a procedure in which a sample of tissue is taken from the affected area and examined under a microscope for cancer cells. This is often the most accurate way to confirm a diagnosis of mucoepidermoid carcinoma.
- Imaging tests: Imaging tests such as computed tomography (CT) scans, magnetic resonance imaging (MRI), and positron emission tomography (PET) scans can be used to assess the size and location of the tumor, as well as to check for any metastases (cancer spread).
- Reverse transcription polymerase chain reaction (RT-PCR): RT-PCR is a laboratory test that can detect specific genetic changes in the tumour cells. This test can help confirm the presence of mucoepidermoid carcinoma.
- Fluorescence in situ hybridization (FISH): FISH is another laboratory test that uses fluorescent probes to identify specific genetic changes in the tumour cells. This test can also help confirm the presence of mucoepidermoid carcinoma.
It's worth noting that a combination of these tests may be used to diagnose mucoepidermoid carcinoma, and not all patients will require all of them. The specific tests used will depend on the individual patient's situation and the guidance of their healthcare provider.
References:
- [6] Diagnosis of mucoepidermoid carcinoma involves physical examination, x-rays, CT, MRI, and biopsy.
- [10] For mucoepidermoid carcinoma, NGS can detect the presence of the MAML2 fusion and other genetic changes. Fluorescence in situ hybridization (FISH): FISH is a laboratory test that uses fluorescent probes to identify specific genetic changes in the tumour cells.
- [11] Mucoepidermoid carcinoma (MEC) is often seen in salivary glands and can harbor MAML2 translocations (MAML2+). The translocation status has diagnostic utility as an objective confirmation of the MEC diagnosis, for example, when distinction from the ...
- [5] by TP Joseph ยท 2015 ยท Cited by 39 โ Recently ancilliary studies like reverse transcription polymerase chain reaction (RT-PCR) and fluorescent in situ hybridization (FISH) have found to be useful ...
Additional Diagnostic Tests
- Biopsy
- Reverse transcription polymerase chain reaction (RT-PCR)
- Fluorescence in situ hybridization (FISH)
- Imaging tests (CT, MRI, PET)
Treatment
Mucoepidermoid carcinoma (MEC) is a type of cancer that affects the salivary glands, and while surgery is often the primary treatment approach, drug therapy can also play a role in managing this disease.
Targeted Biologic Agents
Recent studies have investigated the use of targeted biologic agents, such as trastuzumab, imatinib, and cetuximab, to treat MEC [4]. These drugs are designed to specifically target cancer cells with certain genetic characteristics, reducing harm to healthy tissues. While results are promising, more research is needed to fully understand their efficacy in treating MEC.
Chemotherapy
Conventional chemotherapy has been shown to produce tumor responses in 20-30% of patients with metastatic high-grade MEC or salivary duct carcinoma [8]. However, the effectiveness of chemotherapy can vary depending on individual patient factors and the specific type of MEC being treated. In some cases, chemotherapy may be used as an adjunct to surgery or radiation therapy.
Multitargeted Tyrosine Kinase Inhibitors
For patients with adenoid cystic carcinoma (ACC), a multitargeted tyrosine kinase inhibitor (TKI) such as lenvatinib or sorafenib may be considered for systemic therapy [6]. While not specifically mentioned in the context of MEC, TKIs have shown promise in treating other types of head and neck cancers.
Resistance to Chemotherapy
Interestingly, research has also explored the mechanisms behind resistance to chemotherapy in MEC cells. Studies have found that despite treatment with highly cytotoxic drugs like cisplatin, some MEC cells may exhibit intrinsic mechanisms of resistance [13]. This highlights the need for further investigation into more effective treatment strategies.
Current Treatment Guidelines
While surgery remains the most common approach for resectable tumors, current treatment guidelines for MEC often include surgical resection with eventual adjuvant radiotherapy. Chemotherapy is sometimes reserved for cases where cancer has recurred or spread [12].
In summary, while drug therapy can play a role in managing mucoepidermoid carcinoma, the effectiveness of these treatments can vary depending on individual patient factors and the specific type of MEC being treated. Further research is needed to fully understand the potential benefits and limitations of these approaches.
References:
[1] Context result 2 [4] Context result 4 [8] Context result 8 [12] Context result 12 [13] Context result 13
Recommended Medications
- trastuzumab
- cetuximab
- imatinib
- sorafenib
- lenvatinib
๐ Drug information is sourced from ChEBI (Chemical Entities of Biological Interest) database. Always consult with a healthcare professional before starting any medication. Click on any medication name for detailed information.
Differential Diagnosis
Differential Diagnosis of Mucoepidermoid Carcinoma
Mucoepidermoid carcinoma (MEC) is a type of malignant salivary gland tumor, and its differential diagnosis can be challenging due to its variable histological features. The following entities are considered in the differential diagnosis of MEC:
- Squamous cell carcinoma: This is one of the most common differential diagnoses for MEC, particularly in cases where there is a predominance of epidermoid cells (1).
- Adenoid cystic carcinoma: This type of tumor can also present with mucinous features, making it difficult to distinguish from MEC (4).
- Necrotizing sialometaplasia: This condition can mimic the histological appearance of MEC, particularly in cases where there is a mixture of epidermoid and mucous cells (10).
- Pleomorphic adenoma: This type of benign salivary gland tumor can also present with a mix of epithelial and myoepithelial elements, making it difficult to distinguish from MEC (5).
- Cystadenoma: This type of tumor can also be considered in the differential diagnosis of MEC, particularly in cases where there is a cystic component (8, 10).
Key Features for Differential Diagnosis
To accurately diagnose MEC, it is essential to consider the following key features:
- The presence of mucous cells and epidermoid cells in varying proportions (1, 13)
- The presence of intermediate cells, which can be a mix of epithelial and myoepithelial elements (7, 13)
- The presence of oncocytic cells, clear cells, or spindle cells, which can also be present in MEC (13)
- The absence of a distinct capsule or border, which is more characteristic of benign salivary gland tumors (10)
References
(1) Context result 1 (4) Context result 4 (5) Context result 5 (7) Context result 7 (8) Context result 8 (10) Context result 10 (13) Context result 13
Additional Differential Diagnoses
- tongue squamous cell carcinoma
- bronchus mucoepidermoid carcinoma
- sublingual gland adenoid cystic carcinoma
- lung mucinous cystadenocarcinoma
- salivary gland mucinous adenocarcinoma
- mammary analogue secretory carcinoma
- pleomorphic adenoma carcinoma
- pleomorphic adenoma
- adenosquamous carcinoma
- lung adenoid cystic carcinoma
- trachea adenoid cystic carcinoma
- obsolete basaloid squamous cell carcinoma of the head and neck
Additional Information
- oboInOwl#hasOBONamespace
- disease_ontology
- oboInOwl#id
- DOID:4531
- core#notation
- DOID:4531
- oboInOwl#hasDbXref
- UMLS_CUI:C0206694
- IAO_0000115
- A carcinoma that is characterized by the presence of cuboidal mucous cells, goblet-like mucous cells, squamoid cells, cystic changes, and a fibrotic stromal formation.
- oboInOwl#hasExactSynonym
- MEC
- rdf-schema#label
- mucoepidermoid carcinoma
- oboInOwl#inSubset
- http://purl.obolibrary.org/obo/doid#NCIthesaurus
- rdf-schema#subClassOf
- http://purl.obolibrary.org/obo/DOID_4688
- 22-rdf-syntax-ns#type
- http://www.w3.org/2002/07/owl#Class
- rdf-schema#domain
- https://w3id.org/def/predibionto#has_symptom_3093
- owl#annotatedSource
- t432955
Medical Disclaimer: The information provided on this website is for general informational and educational purposes only.
It is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified healthcare provider with questions about your medical condition.