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Staging for cutaneous T cell lymphoma(Mycosis fungoides (MF) and Sezary syndrome have same critera for staging) is provided in the following table:
Staging for cutaneous T cell lymphoma(Mycosis fungoides (MF) and Sezary syndrome have same critera for staging) is provided in the following table:
{| class="wikitable"
|+
! colspan="2" |Staging for mycosis fungoides and Sezary syndrome
|-
| colspan="2" |Skin(T)
|-
|T1
|Limited patches, papules, and/or plaques covering <10% of the skin surface. May further stratify into T1a (patch only) versus T1b (plaque  patch)
|-
|T2
|Patches, papules, or plaques covering 10% of the skin surface. May further stratify into T2a (patch only) versus T2b (plaque  patch).
|-
|T3
|One or more tumours (1-cm diameter)
|-
|T4
|Confluence of erythema covering 80% body surface area
|-
| colspan="2" |Node(N)
|-
|N0
|No clinically abnormal peripheral lymph nodes; biopsy not required
|-
|N1
|Clinically abnormal lymph nodes; histopathology Dutch grade 1 or NCI LN0-2
|-
|N1a
|Clone negative
|-
|N1b
|Clone posetive
|-
|N2
|Clinically abnormal peripheral lymph nodes; histopathology Dutch grade 2 or NCI LN3
|-
|N2a
|Clone negatove
|-
|N2b
|Clone posetive
|-
|N3
|Clinically abnormal peripheral lymph nodes; histopathology Dutch grades 3e4 or NCI LN4; clone positive or negative
|-
|NX
|Clinically abnormal peripheral lymph nodes; no histologic confirmation
|-
| colspan="2" |Visceral(M)
|-
|M0
|No visceral organ involvement
|-
|M1
|Visceral involvement (must have pathology confirmation and organ involved should be specified)
|-
| colspan="2" |Blood
|-
|B0
|0 Absence of significant blood involvement: �5% of peripheral blood lymphocytes are atypical (Se´zary) cells B0a Clone negative B0b Clone positive
|-
|B1
|Low blood tumour burden: >5% of peripheral blood lymphocytes are atypical (Se´zary) cells but does not meet the criteria of B2 B1a Clone negative B1b Clone positive
|-
|B2
|High blood tumour burden: 1000/mL Se´zary cells with positive clone
|}
The staging of Sezary syndrome is based on the clinical stages:<ref name="TrautingerEder2017" /><ref name="JawedMyskowski2014">{{cite journal|last1=Jawed|first1=Sarah I.|last2=Myskowski|first2=Patricia L.|last3=Horwitz|first3=Steven|last4=Moskowitz|first4=Alison|last5=Querfeld|first5=Christiane|title=Primary cutaneous T-cell lymphoma (mycosis fungoides and Sézary syndrome)|journal=Journal of the American Academy of Dermatology|volume=70|issue=2|year=2014|pages=205.e1–205.e16|issn=01909622|doi=10.1016/j.jaad.2013.07.049}}</ref>


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Revision as of 16:17, 8 November 2018


Mycosis fungoides Microchapters

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sowminya Arikapudi, M.B,B.S. [2], Sogand Goudarzi, MD [3]

Overview

If left untreated, cutaneous T cell lymphoma may progress to develop cutaneous patches, plaque, and tumors. Depending on the extent of the lymphoma at the time of diagnosis, the prognosis may vary.

Natural History

  • Mycosis fungoides is initially an indolent lymphoma that may later develop peripheral lymphadenopathy and can finally progress to widespread visceral involvement.[1]
  • Cutaneous T cell lymphoma is usually initially seen by dermatologists with patients presenting with skin lesions such as erythematous patches or plaque.
  • Patients often have a history of several years of eczematous or dermatitic skin lesions before the diagnosis is finally established.
  • The skin lesions then progress from the patch stage to the plaque stage to cutaneous tumors.

Complications

  • Common complications of Cutaneous T cell lymphoma include:
    • Mycosis Fungoides increased risk of secondary malignancies such as primary malignancy, especially Hodgkin lymphoma, chronic leukemia, and lung cancer.[2]
    • [Complication 2]
    • [Complication 3]

Prognosis

  • Cutaneous T cell lymphoma is usually a slow-growing (indolent) lymphoma.[3]
  • The prognosis for people with cutaneous T cell lymphoma is based on the extent of disease and how the person responds to treatment.
  • Although more advanced stages of cutaneous T cell lymphoma may not be cured, the lymphoma can still be controlled with treatment.

Favorable prognosis

  • Early stage disease
  • Lymphoma is confined to the skin

Unfavorable prognosis

  • More advanced disease
  • Lymphoma has spread to lymph nodes
  • Lymphoma has spread to other organs


Staging

The staging of cutaneous T cell lymphoma is based on skin and lymph node involvement.[3]

Staging for cutaneous T cell lymphoma(Mycosis fungoides (MF) and Sezary syndrome have same critera for staging) is provided in the following table:

Staging for mycosis fungoides and Sezary syndrome
Skin(T)
T1 Limited patches, papules, and/or plaques covering <10% of the skin surface. May further stratify into T1a (patch only) versus T1b (plaque patch)
T2 Patches, papules, or plaques covering 10% of the skin surface. May further stratify into T2a (patch only) versus T2b (plaque patch).
T3 One or more tumours (1-cm diameter)
T4 Confluence of erythema covering 80% body surface area
Node(N)
N0 No clinically abnormal peripheral lymph nodes; biopsy not required
N1 Clinically abnormal lymph nodes; histopathology Dutch grade 1 or NCI LN0-2
N1a Clone negative
N1b Clone posetive
N2 Clinically abnormal peripheral lymph nodes; histopathology Dutch grade 2 or NCI LN3
N2a Clone negatove
N2b Clone posetive
N3 Clinically abnormal peripheral lymph nodes; histopathology Dutch grades 3e4 or NCI LN4; clone positive or negative
NX Clinically abnormal peripheral lymph nodes; no histologic confirmation
Visceral(M)
M0 No visceral organ involvement
M1 Visceral involvement (must have pathology confirmation and organ involved should be specified)
Blood
B0 0 Absence of significant blood involvement: �5% of peripheral blood lymphocytes are atypical (Se´zary) cells B0a Clone negative B0b Clone positive
B1 Low blood tumour burden: >5% of peripheral blood lymphocytes are atypical (Se´zary) cells but does not meet the criteria of B2 B1a Clone negative B1b Clone positive
B2 High blood tumour burden: 1000/mL Se´zary cells with positive clone

The staging of Sezary syndrome is based on the clinical stages:[4][5]

Staging of cutaneous T cell lymphoma [3]
Stage Involvement
stage I
I A
  • Less than 10% of the skin is covered with patches or plaques
I B
  • 10% or more of the skin is covered with patches or plaques
stage II
II A
  • Any amount of the skin is covered in patches or plaques
  • Lymph nodes are enlarged, but do not contain cancer
II B
  • There is one or more raised tumors on the skin
  • Lymph nodes may or may not be enlarged and do not contain cancer
stage III
III
  • Almost all of the skin is reddened
  • There may or may not be patches, plaques or skin tumors
  • Lymph nodes may or may not be enlarged and do not contain cancer
stage IV
IV A
  • Cancer has spread to the lymph nodes, but not to other organs in the body
IV B
  • Cancer has spread to other organs in the body, including the blood and bone marrow
  • Lymph nodes may be enlarged and may contain cancer

References

  1. Mycosis fungoides. Radiopaedia.http://radiopaedia.org/articles/mycosis-fungoides Accessed on January 20, 2016
  2. Cengiz FP, Emiroğlu N, Onsun N (December 2017). "Frequency and Risk Factors for Secondary Malignancies in Patients with Mycosis Fungoides". Turk J Haematol. 34 (4): 378–379. doi:10.4274/tjh.2017.0234. PMC 5774354. PMID 28832009.
  3. 3.0 3.1 3.2 Cutaneous T cell lymphoma. Canadian Cancer Society. http://www.cancer.ca/en/cancer-information/cancer-type/non-hodgkin-lymphoma/non-hodgkin-lymphoma/types-of-nhl/cutaneous-t-cell-lymphoma/?region=on Accessed on January 19, 2016
  4. Jawed, Sarah I.; Myskowski, Patricia L.; Horwitz, Steven; Moskowitz, Alison; Querfeld, Christiane (2014). "Primary cutaneous T-cell lymphoma (mycosis fungoides and Sézary syndrome)". Journal of the American Academy of Dermatology. 70 (2): 205.e1–205.e16. doi:10.1016/j.jaad.2013.07.049. ISSN 0190-9622.


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