Sandbox: T-cell large granular lymphocyte leukemia: Difference between revisions

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== Diagnosis ==
== Diagnosis ==
===Diagnostic Criteria===
===Diagnostic Criteria===
*The diagnosis of T-cell large granular lymphocyte leukemia is made when at least [number] of the following [number] diagnostic criteria are met:
*The diagnosis of T-cell large granular lymphocyte leukemia is made when the following diagnostic criteria is met:
:*Clonal rearrangements of the [[T-cell receptor]] (TCR) genes
:*Clonal rearrangements of the [[T-cell receptor]] (TCR) gene
:*[criterion 2]
:*Chronic (> 6 months) elevation in large granular lymphocytes (LGLs) in the peripheral blood
:*[criterion 3]
:*[criterion 3]
:*[criterion 4]
:*[criterion 4]
 
=== Symptoms ===
=== Symptoms ===
*T-cell large granular lymphocyte leukemia is usually asymptomatic.
*T-cell large granular lymphocyte leukemia is usually asymptomatic.

Revision as of 15:15, 28 April 2016

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [2] Associate Editor(s)-in-Chief: Raviteja Guddeti, M.B.B.S. [3] Maria Fernanda Villarreal, M.D. [4]

Synonyms and keywords: LGL leukemia; Tγ-lymphoproliferative disorder; T-cell chronic lymphocytic leukemia; proliferation of large granular lymphocytes (LGLs)

Overview

T-cell large granular lymphocyte leukemia (also known as T-GLL) is a rare type of leukemia that exhibits a unexplained, chronic (> 6 months) elevation in large granular lymphocytes (LGLs) in the peripheral blood.[1]

Historical Perspective

  • T-cell large granular lymphocyte leukemia was first discovered by [scientist name], a [nationality + occupation], in [year] during/following [event].

Classification

  • T-cell large granular lymphocyte leukemia may be classified into 2 groups:
  • T-cell large granular lymphocyte leukemia (T-LGL)
  • Natural-killer (NK) granular lymphocyte leukemia (NK-LGL)
  • Other variants of T-cell large granular lymphocyte leukemia include

Pathophysiology

  • The pathogenesis of T-cell large granular lymphocyte leukemia is characterized by involvement of cytotoxic-T cells.
  • The postulated cells of origin of T-LGL leukemia are transformed CD8+ T-cell with clonal rearrangements of β chain T-cell receptor genes for the majority of cases and a CD8- T-cell with clonal rearrangements of γ chain T-cell receptor genes for a minority of cases.
  • The [gene name] gene/Mutation in [gene name] has been associated with the development of T-cell large granular lymphocyte leukemia, involving the [molecular pathway] pathway.
  • On gross pathology, characteristic findings of T-cell large granular lymphocyte leukemia, include:
  • On microscopic histopathological analysis, characteristic findings of T-cell large granular lymphocyte leukemia, include:

Causes

  • Common causes of T-cell large granular lymphocyte leukemia, include:

Differentiating T-cell Large Granular Lymphocyte Leukemia from Other Diseases

  • T-cell large granular lymphocyte leukemia must be differentiated from other diseases that cause [clinical feature 1], [clinical feature 2], and [clinical feature 3], such as:

Epidemiology and Demographics

  • T-cell large granular lymphocyte leukemia is a rare form of leukemia, comprising 2-3% of all cases of chronic lymphoproliferative disorders.

Age

  • Patients of all age groups may develop T-cell large granular lymphocyte leukemia.
  • T-cell large granular lymphocyte leukemia is more commonly observed among patients aged [age range] years old.
  • T-cell large granular lymphocyte leukemia is more commonly observed among middle aged adults.

Gender

  • T-cell large granular lymphocyte leukemia affects men and women equally.

Race

  • There is no racial predilection for T-cell large granular lymphocyte leukemia.

Risk Factors

  • Common risk factors in the development of T-cell large granular lymphocyte leukemia, include:

Natural History, Complications and Prognosis

  • The majority of patients with T-cell large granular lymphocyte leukemia may be initially asymptomatic.
  • Early clinical features include
  • If left untreated, patients with T-cell large granular lymphocyte leukemia may progress to develop infections.
  • Common complications of T-cell large granular lymphocyte leukemia, include:
  • Prognosis is generally good, and the 5 year survival rate of patients with T-cell large granular lymphocyte leukemia is approximately 89%.

Diagnosis

Diagnostic Criteria

  • The diagnosis of T-cell large granular lymphocyte leukemia is made when the following diagnostic criteria is met:
  • Clonal rearrangements of the T-cell receptor (TCR) gene
  • Chronic (> 6 months) elevation in large granular lymphocytes (LGLs) in the peripheral blood
  • [criterion 3]
  • [criterion 4]

Symptoms

  • T-cell large granular lymphocyte leukemia is usually asymptomatic.
  • Symptoms of T-cell large granular lymphocyte leukemia may include the following:
  • [symptom 1]
  • [symptom 2]
  • [symptom 3]

Physical Examination

  • Patients with T-cell large granular lymphocyte leukemia usually appear pale and malnourished.
  • Physical examination may be remarkable for:
  • [finding 1]
  • [finding 2]
  • [finding 3]
  • [finding 4]
  • [finding 5]
  • [finding 6]

Laboratory Findings

  • Laboratory findings consistent with the diagnosis of T-cell large granular lymphocyte leukemia, include:

Imaging Findings

  • There are no specific imaging findings associated with T-cell large granular lymphocyte leukemia.

Other Diagnostic Studies

  • T-cell large granular lymphocyte leukemia may also be diagnosed using the following studies:

Treatment

Medical Therapy

  • The mainstay of therapy for T-cell large granular lymphocyte leukemia is [medical therapy 1] and [medical therapy 2].

Surgery

  • Surgery is the mainstay of therapy for T-cell large granular lymphocyte leukemia.
  • [Surgical procedure] in conjunction with [chemotherapy/radiation] is the most common approach to the treatment of T-cell large granular lymphocyte leukemia.
  • [Surgical procedure] can only be performed for patients with [disease stage] T-cell large granular lymphocyte leukemia.

Prevention

  • There are no primary preventive measures available for T-cell large granular lymphocyte leukemia.
  • Once diagnosed and successfully treated, patients with T-cell large granular lymphocyte leukemia are followed-up every [duration]. Follow-up testing includes [test 1], [test 2], and [test 3].

References

  1. [1] Jaffe E.S., Harris N.L., Stein H., Vardiman J.W. (eds): World Health Organization Classification of Tumors. Pathology and Genetics of Tumours of Haemopoietic and Lymphoid Tissues. IARC Press: Lyon 2001