4 free views remaining today

ameloblastoma

ICD-10 Codes

Related ICD-10:

Description

Ameloblastoma is a rare and slow-growing tumor that usually forms in the lower jaw, specifically in the space behind the back teeth [2]. It is a benign (non-cancerous) tumor that arises from the enamel tissue of the tooth, which has not undergone differentiation [4].

The clinical signs of ameloblastoma may be subtle at first, but as the lesion advances in size, symptoms such as pain and disfigurement may become apparent [5]. Ameloblastomas are locally aggressive benign tumors that arise from the mandible (lower jaw) or, less commonly, from the maxilla (upper jaw) [7].

Ameloblastoma is a rare tumor, representing about 1% of all jaw tumors, and it can appear to be solid or cyst-like in nature [3]. It is more commonly found in the lower jaw than the upper jaw [6]. The growth rate of ameloblastoma is slow, and it may take several years for the tumor to become noticeable.

In terms of its appearance, ameloblastoma can cause a slow-growing, painless swelling of the jaw. As the lesion advances, increased size often relates to more clinically significant symptoms [8].

It's worth noting that ameloblastoma is the most common benign tumour of odontogenic origin in Africa and presents five times more in the mandible than the maxilla [9].

Additional Characteristics

  • A rare and slow-growing tumor
  • Forms in the lower jaw, behind the back teeth
  • Benign (non-cancerous) tumor from enamel tissue
  • Locally aggressive benign tumors
  • Rare, representing about 1% of all jaw tumors
  • Can appear solid or cyst-like
  • More common in lower jaw than upper jaw
  • Slow growth rate, taking years to become noticeable
  • Causes slow-growing, painless swelling of the jaw

Signs and Symptoms

Common Signs and Symptoms of Ameloblastoma

Ameloblastoma, a rare jaw tumor, can manifest in various ways. The following are the most commonly reported symptoms:

  • Painless swelling: A lump or swelling in the jaw area is often the first sign of ameloblastoma [6].
  • Bone pain: Some individuals may experience pain in the affected bone, although this is not a common symptom [2].
  • Abnormal growth: An abnormal growth in the jaw or sinus area can be a sign of ameloblastoma [1].
  • Facial disfigurement: If left untreated, ameloblastomas can become large lesions causing facial disfigurement and dental malocclusion [5].

It's essential to note that these symptoms may not always be present, and the tumor can grow slowly over many months or even years before being detected [3]. In some cases, the only symptom may be swelling in the back of the jaw [4].

References:

[1] Context result 2 [2] Context result 2 [3] Context result 3 [4] Context result 4 [5] Context result 5 [6] Context result 6

Additional Symptoms

  • Painless swelling
  • Abnormal growth
  • Facial disfigurement
  • bone pain

Diagnostic Tests

Diagnostic Tests for Ameloblastoma

Ameloblastoma, a rare and benign tumor that affects the jawbone, can be diagnosed using various imaging tests and biopsies. Here are some of the diagnostic tests used to confirm the presence of ameloblastoma:

  • Imaging tests: X-rays, computed tomography (CT) scans, and magnetic resonance imaging (MRI) scans help doctors determine the extent of an ameloblastoma. These tests can sometimes find the tumor on routine X-rays at the dentist's office [5][6].
  • Panoramic radiography: This test is often used to detect ameloblastoma, along with CT scans and MRI scans [3][4].
  • Fine-needle aspiration cytology (FNAC): While not always necessary, FNAC can be used to confirm the diagnosis of ameloblastoma by examining a sample of cells from the tumor [4].
  • Biopsy: A biopsy of the bone is usually required to confirm the presence of ameloblastoma and rule out other conditions [7][9].

It's essential to note that a combination of imaging techniques and a biopsy are often used to diagnose ameloblastoma, as this provides the most accurate information about the tumor's size, location, and extent [9].

Additional Diagnostic Tests

  • X-rays
  • computed tomography (CT) scans
  • magnetic resonance imaging (MRI) scans
  • panoramic radiography
  • fine-needle aspiration cytology (FNAC)
  • biopsy

Treatment

Treatment Options for Ameloblastoma

Ameloblastoma, a rare type of tumor that affects the jawbone, can be treated with various methods depending on its size, location, and type. According to recent studies [3], treatment may involve targeted therapy using anti-BRAF inhibitors or MEK inhibitors.

Targeted Therapy

Research has shown that targeted therapy is an effective treatment option for ameloblastoma [6]. Anti-MAPK targeted therapy, in particular, has been found to be safe and efficient in treating primary, recurrent, or metastasizing ameloblastomas [6].

  • BRAF inhibitors, such as vemurafenib and dabrafenib, have been approved for the treatment of BRAF mutation-positive tumors [1].
  • MEK inhibitors, like trametinib, can be used in combination with BRAF inhibitors to enhance treatment efficacy [4].

Surgical Intervention

While targeted therapy is a promising approach, surgery remains the best treatment option for ameloblastoma. According to medical experts [9], surgical removal of the tumor and surrounding tissue is often necessary to ensure no abnormal cells remain.

  • Surgery can be performed by experienced healthcare providers who specialize in oral and maxillofacial surgery.
  • The goal of surgery is to remove the tumor completely, thereby preventing recurrence and promoting healing.

Other Treatment Options

In some cases, treatment may involve a combination of targeted therapy and surgery. For instance, if the tumor is large or has spread to other areas, surgical removal followed by targeted therapy may be necessary [7].

  • It's essential to consult with a healthcare provider who specializes in oral and maxillofacial surgery to determine the best course of treatment.
  • A multidisciplinary team approach can ensure that patients receive comprehensive care tailored to their specific needs.

References

[1] K Heikinheimo · 2015 · Cited by 78 — Selective inhibitors of mutated BRAF, vemurafenib and dabrafenib, as well as the MEK inhibitor trametinib, have been approved for the treatment of BRAF mutation ...

[3] Oct 12, 2024 — Ameloblastoma treatment may depend on your tumor's size and location, and the type and appearance of the cells involved.

[4] by S Grynberg · 2024 · Cited by 8 — The treatment protocol for these tumors may involve BRAF inhibitors alone or in combination with MEK inhibitors. Although data from metastatic melanoma patients ...

[6] by A Raemy · 2024 — Anti-MAPK targeted therapy seems to be safe and efficient in treating ameloblastoma that is primary, recurrent, or metastasizing. It allows for a clinical, ...

[9] Surgery that removes the tumor and some nearby tissue (enough to ensure no abnormal cells remain) is the best treatment for ameloblastoma. Healthcare providers ...

Recommended Medications

💊 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 Ameloblastoma

Ameloblastoma, also known as odontogenic epithelial tumor, is a rare and benign tumor that arises from the epithelial cells of the jawbone. However, differentiating it from other dental and bone-related conditions can be challenging. Here are some key points to consider:

  • Differential diagnosis: Ameloblastoma must be differentiated from other odontogenic tumors such as dentigerous cyst, odontogenic keratocyst (OKC), odontogenic myxoma, aneurysmal bone cyst (ABC), fibrous dysplasia, and giant cell reparative granuloma [1].
  • Histological features: While histology alone may not be sufficient to differentiate ameloblastoma from malignant tumors, certain characteristics such as the presence of a follicular or plexiform pattern can aid in diagnosis [2].
  • Imaging studies: Radiographic and CT findings are essential for differentiating ameloblastoma from other conditions. Cortical dilation and perforation are significant differential diagnostic points that cannot be observed on panoramic radiographs [4].
  • Diagnostic accuracy: Studies have shown a relatively high rate of diagnostic accuracy (92.8%) using CT findings to differentiate OKC and ameloblastoma [6].

Key Points to Consider

  • Ameloblastoma must be differentiated from other odontogenic tumors.
  • Histological features, imaging studies, and diagnostic criteria are essential for accurate diagnosis.
  • Cortical dilation and perforation are significant differential diagnostic points.

References

[1] JC Palanisamy (2023) - Differential Diagnosis of Ameloblastoma [2] Z Liu (2021) - The differentiation of the ameloblastoma and odontogenic keratocyst directly affects the formulation of surgical plans, while the results of ... [4] K Hu (2024) - Cortical dilation and perforation are two significant differential diagnostic points that cannot be observed on panoramic radiographs of ameloblastoma (... [6] N Kaneko (2023) - Our criteria for differential diagnosis between OKC and ameloblastoma using CT findings resulted in a relatively high rate of diagnostic accuracy (92.8 %); ...

Additional Differential Diagnoses

Additional Information

rdf-schema#domain
https://w3id.org/def/predibionto#has_symptom_928
owl#annotatedSource
t336473
core#notation
DOID:0050894
core#exactMatch
MESH:D000564
rdf-schema#label
ameloblastoma
rdf-schema#subClassOf
http://purl.obolibrary.org/obo/DOID_0060084
22-rdf-syntax-ns#type
http://www.w3.org/2002/07/owl#Class
owl#equivalentClass
t336390
oboInOwl#hasOBONamespace
disease_ontology
oboInOwl#created_by
lschriml
oboInOwl#creation_date
2014-09-11T02:44:50Z
oboInOwl#id
DOID:0050894
oboInOwl#hasDbXref
MESH:D000564
IAO_0000115
A cell type benign neoplasm that has_material_basis_in odontogenic epithelium.
oboInOwl#inSubset
http://purl.obolibrary.org/obo/doid#DO_rare_slim
relatedICD
http://example.org/icd10/D11.7

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.