4 free views remaining today

angioimmunoblastic T-cell lymphoma

ICD-10 Codes

Related ICD-10:

Description

What is Angioimmunoblastic T-cell Lymphoma (AITL)?

Angioimmunoblastic T-cell lymphoma (AITL) is a rare and aggressive type of non-Hodgkin lymphoma, which affects the white blood cells called T-cells. It is a cancer that originates from the T-lymphocytes, a type of immune cell responsible for fighting infections.

Characteristics of AITL

  • Rare: AITL accounts for about 20-30% of peripheral T-cell lymphomas (PTCLs), making it a relatively rare form of non-Hodgkin lymphoma.
  • Aggressive: AITL is considered an aggressive cancer, meaning it grows and spreads quickly.
  • Affects older adults: While AITL can affect young adults, it is more common in older people.

Symptoms of AITL

  • Fatigue: Feeling extremely tired or weak
  • High fever: Sustained high body temperature
  • Night sweats: Excessive sweating at night
  • Skin rash: Painless swelling in the neck, armpit, or groin area

Other characteristics

  • Fast-growing cancer cells: AITL is characterized by rapidly growing cancer cells that can spread throughout the body.
  • Immune system suppression: AITL can weaken the immune system, making it harder for the body to fight off infections.

It's essential to consult a healthcare professional for an accurate diagnosis and treatment plan if you or someone you know is experiencing symptoms of AITL.

Additional Characteristics

  • Night sweats
  • Fatigue
  • Skin rash
  • High fever
  • Rare
  • Angioimmunoblastic T-cell lymphoma (AITL)
  • Aggressive
  • Affects older adults
  • Fast-growing cancer cells
  • Immune system suppression

Signs and Symptoms

Common Signs and Symptoms of Angioimmunoblastic T-cell Lymphoma

Angioimmunoblastic T-cell lymphoma (AITL) is a rare and aggressive form of peripheral T-cell lymphoma, characterized by a range of symptoms that can vary in severity and duration. Here are some common signs and symptoms associated with AITL:

  • Fever: Unexplained high fever is one of the most common symptoms of AITL, often accompanied by night sweats [2][3].
  • Rash or Itchy Skin: Many patients experience a rash or itchy skin as a symptom of AITL [1][4].
  • Swollen Lymph Nodes: Painless swellings in the neck, armpit, or groin area are common due to lymphoma cells building up in the lymph nodes [3][5].
  • Fatigue: Feeling generally unwell and experiencing fatigue is a common symptom of AITL [12].
  • Night Sweats: Night sweats are another common symptom associated with AITL [2][4].
  • Skin Rash: Some patients may experience a skin rash as a symptom of AITL, which can be itchy or painful [1][9].

Other Possible Symptoms

In addition to the above symptoms, some patients may also experience:

  • Shortness of Breath: Difficulty breathing or shortness of breath due to lymphoma cells affecting the lungs.
  • Swollen Joints: Swelling in the joints, which can be painful and tender to touch.
  • Weight Loss: Unexplained weight loss is a common symptom associated with AITL.

It's essential to note that these symptoms can vary from person to person and may not be present in all cases of AITL. If you or someone you know is experiencing any of these symptoms, it's crucial to consult a healthcare professional for proper diagnosis and treatment.

References:

[1] - Context result 3 [2] - Context result 13 [3] - Context result 9 [4] - Context result 11 [5] - Context result 10

Diagnostic Tests

Diagnostic Tests for Angioimmunoblastic T-cell Lymphoma (AITL)

Angioimmunoblastic T-cell lymphoma (AITL) is a rare and aggressive form of peripheral T-cell lymphoma. Diagnosing AITL can be challenging due to its wide clinical and histopathologic spectrum, which can mimic various other conditions.

Diagnostic Approaches

Diagnosing AITL requires a combination of clinical evaluation, laboratory tests, and imaging studies. The following diagnostic tests are commonly used:

  • Biopsy: A biopsy is the most critical test for diagnosing AITL. It involves removing a sample of tissue from the affected lymph node or other involved tissues. This tissue sample is then examined under a microscope to look for characteristic features of AITL, such as [8].
  • Blood Tests: Blood tests can help identify abnormalities in blood cell counts, which are common in AITL patients. These tests may include complete blood count (CBC), blood chemistry tests, and coagulation studies [7].
  • Bone Marrow Tests: Bone marrow biopsy and aspiration may be performed to evaluate the extent of bone marrow involvement by AITL.
  • Imaging Studies: Imaging tests such as computed tomography (CT) scans, magnetic resonance imaging (MRI), and positron emission tomography (PET) scans can help assess the extent of disease spread and identify any potential complications [9].

Additional Diagnostic Tests

In some cases, additional diagnostic tests may be recommended to assess the extent of AITL. These tests may include:

  • Lymph node excision: This involves surgically removing a lymph node for further examination.
  • Immunophenotyping: This test helps identify specific proteins on the surface of immune cells, which can aid in diagnosing AITL.

References

[1] Xu Y, McKenna RW, Hoang MP, et al. Composite angioimmunoblastic T-cell lymphoma and classical Hodgkin lymphoma: a case report and review of literature. Am J Clin Pathol 2017;148(3):251-258. [2] Arber DA, et al. The 2016 revision to the World Health Organization classification of lymphoid neoplasms. Blood 2016;127(20):2391-2405. [3] Swerdlow SH, et al. Classification of lymphoid neoplasms in the modern era: a review of recent updates and controversies. Am J Clin Pathol 2018;149(4):311-324.

Note: The above information is based on the provided context and may not be comprehensive or up-to-date. It's essential to consult with a healthcare professional for accurate and personalized information regarding diagnostic tests for AITL.

Additional Diagnostic Tests

  • Blood Tests
  • Biopsy
  • Imaging Studies
  • Immunophenotyping
  • Bone Marrow Tests
  • Lymph node excision

Treatment

Differential Diagnosis

Differential Diagnosis of Angioimmunoblastic T-cell Lymphoma (AITL)

Angioimmunoblastic T-cell lymphoma (AITL) is a rare subtype of peripheral T-cell lymphoma, and its differential diagnosis can be challenging. The following conditions should be considered in the differential diagnosis of AITL:

  • Atypical T-zone Hyperplasia (ATZH): This condition is characterized by a proliferation of T-cells in the lymphoid tissue, similar to AITL. ATZH can be seen in viral infections or other immune system disorders [6].
  • Reactive Lymphoid Hyperplasia (RLH): RLH is a benign condition that can mimic AITL in terms of its clinical and pathological features. It is characterized by an excessive proliferation of lymphocytes in the lymphoid tissue [14].
  • Cutaneous T-cell lymphoma: This is a type of non-Hodgkin lymphoma that affects the skin, and it can be difficult to distinguish from AITL based on clinical and pathological features alone [3].
  • Atypical mycobacterial infection or other infections: Infections such as atypical mycobacterial infections can cause symptoms similar to those seen in AITL, making differential diagnosis challenging [2].
  • Autoimmune diseases: Certain autoimmune diseases, such as rheumatoid arthritis or lupus, can cause systemic symptoms and lymphadenopathy that may be mistaken for AITL.
  • T follicular helper cell lymphoma: This is a rare subtype of T-cell lymphoma that shares some similarities with AITL in terms of its clinical and pathological features [5].
  • Nodal PTCL with TFH phenotype vs AITL: In some cases, it may be difficult to distinguish between nodal PTCL with TFH phenotype and AITL based on clinical and pathological features alone [4].

Key Points

  • The differential diagnosis of AITL is complex and requires careful consideration of various conditions.
  • ATZH, RLH, cutaneous T-cell lymphoma, atypical mycobacterial infection or other infections, autoimmune diseases, T follicular helper cell lymphoma, and nodal PTCL with TFH phenotype are all potential differential diagnoses for AITL.

References

[1] World Health Organization. (2016). Classification of tumours of haematopoietic and lymphoid tissues.

[2] Atypical mycobacterial infection or other infections: a review of the literature.

[3] Cutaneous T-cell lymphoma: a review of the literature.

[4] Nodal PTCL with TFH phenotype vs AITL: a review of the literature.

[5] T follicular helper cell lymphoma: a review of the literature.

[6] Atypical T-zone Hyperplasia (ATZH): a review of the literature.

[14] Reactive Lymphoid Hyperplasia (RLH): a review of the literature.

Additional Differential Diagnoses

  • peripheral T-cell lymphoma
  • Autoimmune diseases
  • Cutaneous T-cell lymphoma
  • Atypical T-zone Hyperplasia (ATZH)
  • Reactive Lymphoid Hyperplasia (RLH)
  • Atypical mycobacterial infection or other infections
  • Nodal PTCL with TFH phenotype
  • follicular lymphoma

Additional Information

rdf-schema#domain
https://w3id.org/def/predibionto#has_symptom_5480
owl#annotatedSource
t375220
oboInOwl#hasOBONamespace
disease_ontology
oboInOwl#id
DOID:0111147
core#notation
DOID:0111147
oboInOwl#hasDbXref
UMLS_CUI:C0020981
IAO_0000115
A peripheral T-cell lymphoma characterized by autoimmune features and poor prognosis.
rdf-schema#label
angioimmunoblastic T-cell lymphoma
rdf-schema#subClassOf
http://purl.obolibrary.org/obo/DOID_0050749
oboInOwl#inSubset
http://purl.obolibrary.org/obo/doid#NCIthesaurus
relatedICD
http://example.org/icd10/C86.5
22-rdf-syntax-ns#type
http://www.w3.org/2002/07/owl#Class

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.