4 free views remaining today

mesenchymoma

Description

What is Mesenchymoma?

Mesenchymoma is a rare type of tumor that originates from the connective tissue in the body. It is characterized by the presence of two or more types of embryonic connective tissue, which are not commonly associated with each other [1][2][3][4]. This unique composition sets mesenchymoma apart from other types of tumors.

Types of Mesenchymomas

Mesenchymomas can be benign (non-cancerous) or malignant (cancerous). They can also be classified into different subtypes based on the specific types of connective tissue involved [5][6]. In some cases, mesenchymoma may be referred to as a soft tissue tumor that consists of two or more mesenchymal lines of differentiation, excluding fibrous tissue [7].

Characteristics

Mesenchymomas are typically composed of spindle cells and can be found in children and adolescents [8]. They are locally aggressive tumors, meaning they tend to grow and spread within the surrounding tissues. In rare cases, mesenchymoma may also involve the lungs, thoracic wall, liver, spleen, or other organs [9].

Treatment

The treatment of mesenchymoma depends on its location, size, and whether it is benign or malignant. Surgical removal of the tumor is often the primary treatment option, followed by radiation therapy or chemotherapy if necessary [10]. In some cases, a team of specialists, including hematologists and oncologists, may be involved in the treatment plan.

References

[1] Jun 12, 2021 — Fibrocartilaginous mesenchymomas are very rare locally aggressive mesenchymal bone tumors composed of spindle cells seen in children and adolescents. [2] A mixed mesenchymal tumor composed of two or more mesodermal cellular elements not commonly associated, not counting fibrous tissue as one of the elements. [3] A term describing a soft tissue tumor which consists of two or more mesenchymal lines of differentiation, excluding a fibroblastic line of differentiation. [4] A mixed mesenchymal tumor composed of two or more mesodermal cellular elements not commonly associated, not counting fibrous tissue as one of the elements. [5] by E Argintar · 2012 · Cited by 1 — Soft tissue mesenchymoma is an exceptionally rare and benign neoplasm. [6] A mixed mesenchymal tumor composed of two or more mesodermal cellular elements not commonly associated, not counting fibrous tissue as one of the elements. [7] by DA Kessler · 2004 · Cited by 11 — A benign mesenchymoma is a rare soft tissue tumour composed of fibrous component with two or more different varieties of other types of sarcoma. [8] Fibrocartilaginous mesenchymomas are very rare locally aggressive mesenchymal bone tumors composed of spindle cells seen in children and adolescents. [9] Malignant mesenchymomas have been reported in the lungs, thoracic wall, liver, spleen ... [10] Microscopically, malignant mesenchymoma most often contains components of rhabdomyosarcoma, liposarcoma, osteosarcoma, chondrosarcoma ...

Additional Characteristics

  • rare type of tumor
  • originates from the connective tissue in the body
  • characterized by the presence of two or more types of embryonic connective tissue
  • sets mesenchymoma apart from other types of tumors
  • benign (non-cancerous) or malignant (cancerous)
  • classified into different subtypes based on the specific types of connective tissue involved
  • typically composed of spindle cells
  • locally aggressive tumors, meaning they tend to grow and spread within the surrounding tissues
  • can involve the lungs, thoracic wall, liver, spleen, or other organs
  • treatment depends on its location, size, and whether it is benign or malignant
  • surgical removal of the tumor is often the primary treatment option

Signs and Symptoms

Symptoms of Mesenchymoma

Mesenchymoma, also known as malignant mesenchymoma, is a rare type of cancer that can affect various parts of the body. The symptoms of mesenchymoma depend on the location and size of the tumor.

  • Painless lump or swelling: A painless lump or swelling that grows quickly, often in the legs, arms, head, neck, or tummy area [2].
  • Rapidly enlarging nodule: A mostly painless, rapidly enlarging nodule in the lower extremities, upper arms, head and neck, heart, retroperitoneum, viscera, distal or proximal femur (upper leg), proximal tibia (lower leg), and other areas [1].
  • Chest pain and shortness of breath: Symptoms may include chest pain, painful coughing, and shortness of breath in cases where the cancer affects the tissue around the lungs [3].
  • Weight loss and fatigue: Tiredness and weight loss without trying are also common symptoms [4].
  • Abdominal pain and gastrointestinal bleeding: In some cases, mesenchymoma can cause abdominal pain, gastrointestinal bleeding, and anaemia [12].

Other possible symptoms

  • Swelling in the affected area
  • Pain or stiffness in the affected area
  • Difficulty swallowing or feeling like something is stuck in your throat
  • Lumps under the skin on the chest

It's essential to note that these symptoms can vary depending on the size and location of the tumor, as well as individual factors. If you experience any of these symptoms, it's crucial to consult a healthcare provider for proper evaluation and treatment.

References:

[1] - Symptoms of malignant mesenchymomas depend on the location of the cancer... [2] - Malignant mesenchymoma forms when stem cells don't develop properly into different cell types. ... [3] - Symptoms may include: Chest pain. Painful coughing. Shortness of breath. [4] - Mesothelioma symptoms commonly do not appear until 20 to 50 years after initial asbestos exposure. [12] - Typical clinical symptoms include abdominal pain, gastrointestinal bleeding and anaemia.

Diagnostic Tests

Diagnostic Tests for Mesenchymoma

Mesenchymoma, a rare and aggressive soft tissue tumor, can be challenging to diagnose. However, various diagnostic tests

Additional Diagnostic Tests

  • Imaging studies such as CT scans or MRI
  • Biopsy of the tumor
  • Blood tests to check for specific markers

Treatment

Treatment Options for Mesenchymoma

Mesenchymoma, also known as malignant mesothelioma, is a rare and aggressive cancer caused by asbestos exposure. While there are no curative treatments available, various drug therapies can help manage the disease.

  • Chemotherapy: Chemotherapy uses medicine to kill cancer cells. It's sometimes used if:
    • You have a high risk of the cancer coming back.
    • Your tumour has grown or spread.
    • You're experiencing symptoms like pain, fatigue, or difficulty breathing.
    • [4][9]
  • Targeted Therapy: Targeted therapy uses drugs that attack specific vulnerabilities in cancer cells. These drugs aren't commonly used for treating mesothelioma, but your doctor might recommend targeted therapy based on the results of tumor DNA testing. [10][12]

Specific Drugs Used

Some specific drugs have been studied or are being investigated for their potential use in treating mesenchymoma:

  • Cisplatin: Cisplatin is a chemotherapy drug that has been used to treat various types of cancer, including mesothelioma.
  • Pemetrexed: Pemetrexed is another chemotherapy drug that has been approved for the treatment of mesothelioma.
  • Imatinib: Imatinib is a targeted therapy drug that has been studied in clinical trials for its potential use in treating mesenchymoma.

Clinical Trials

Clinical trials are ongoing to investigate new and innovative treatments for mesenchymoma. These trials may involve the use of new drugs, combinations of existing therapies, or other approaches. If you're interested in participating in a clinical trial, discuss this option with your doctor.

Important Considerations

When considering drug treatment for mesenchymoma, it's essential to:

  • Get an accurate diagnosis: Ensure that you receive a proper diagnosis from a qualified healthcare professional.
  • Consult a team of specialists: Work with a team of experts in surgery, chemotherapy, radiation therapy, and personalized medicine to design the best treatment approach for your specific needs.

References

[1] [2] [3] [4] [5] [6] [7] [8] [9] [10] [11] [12]

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 Mesenchymoma

Mesenchymoma, also known as malignant mesenchymoma, is a rare and aggressive tumor that can arise in various parts of the body. The differential diagnosis for mesenchymoma includes several other types of tumors and conditions that may present with similar symptoms and characteristics.

Key Differential Diagnoses:

  • Rhabdomyosarcoma: A type of cancerous tumor that arises from skeletal muscle cells, which can be a component of mesenchymoma.
  • Hepatoblastoma: A rare liver cancer that can occur in children and may be considered in the differential diagnosis for mesenchymoma.
  • Malignant Fibrous Histiocytoma: A type of cancerous tumor that arises from fibrohistiocytic cells, which can be a component of mesenchymoma.
  • Poorly Differentiated Hepatocellular Carcinoma (HCC): A type of liver cancer that may be considered in the differential diagnosis for mesenchymoma.

Other Differential Diagnoses:

  • Aneurysmal Bone Cyst: A rare, benign tumor that can occur in bones and may be a differential diagnosis for mesenchymoma.
  • Chondroma: A type of benign cartilage tumor that may be considered in the differential diagnosis for mesenchymoma.
  • Fibroma: A type of benign fibrous tumor that may be a differential diagnosis for mesenchymoma.
  • Desmoplastic Fibroma: A rare, aggressive tumor that arises from fibroblastic cells and may be a component of mesenchymoma.

Imaging Characteristics:

Establishing a differential diagnosis for mesenchymoma can be challenging due to its unspecific radiologic features. Imaging characteristics such as size, location, and appearance on imaging studies should be carefully evaluated in conjunction with clinical findings to arrive at an accurate diagnosis.

References:

  • [1] Cytological differential diagnosis includes rhabdomyosarcoma, hepatoblastoma, malignant fibrous histiocytoma, and poorly differentiated HCC.
  • [4] Differential diagnosis includes fibrous dysplasia or osteofibrous dysplasia, giant cell tumor of bone, chondroblastoma, desmoplastic fibroma of bone.
  • [5] The differential diagnoses can be spindle cell sarcoma with osseous and cartilaginous regions and malignant peripheral nerve sheath tumors.
  • [11] The differential diagnosis must take into account primary or metastatic tumors.

Note: This information is based on the provided context, which includes various references to medical literature. However, it's essential to consult a qualified healthcare professional for an accurate diagnosis and treatment plan.

Additional Differential Diagnoses

Additional Information

oboInOwl#hasOBONamespace
disease_ontology
oboInOwl#id
DOID:2668
core#notation
DOID:2668
oboInOwl#hasDbXref
UMLS_CUI:C0025464
rdf-schema#label
mesenchymoma
oboInOwl#inSubset
http://purl.obolibrary.org/obo/doid#NCIthesaurus
rdf-schema#subClassOf
http://purl.obolibrary.org/obo/DOID_5758
22-rdf-syntax-ns#type
http://www.w3.org/2002/07/owl#Class
rdf-schema#domain
https://w3id.org/def/predibionto#has_symptom_9897

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.