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Research ArticleOriginal Article
Open Access

Differentiating mycosis fungoides lesions from their mimickers clinically and histologically

A single tertiary center retrospective analysis in Saudi Arabia

Fatimah M. Budair, Ahmed A. Alsayyah and Omar M. Alakloby
Saudi Medical Journal December 2024, 45 (12) 1355-1367; DOI: https://doi.org/10.15537/smj.2024.45.12.20240796
Fatimah M. Budair
From the Department of Dermatology (Budair, Al-akloby) and from the Department of Pathology (Alsayyah), King Fahd University Hospital, Alkhobar, College of Medicine, Imam Abdulrahman bin Faisal University, Dammam, Kingdom of Saudi Arabia
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  • ORCID record for Fatimah M. Budair
Ahmed A. Alsayyah
From the Department of Dermatology (Budair, Al-akloby) and from the Department of Pathology (Alsayyah), King Fahd University Hospital, Alkhobar, College of Medicine, Imam Abdulrahman bin Faisal University, Dammam, Kingdom of Saudi Arabia
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Omar M. Alakloby
From the Department of Dermatology (Budair, Al-akloby) and from the Department of Pathology (Alsayyah), King Fahd University Hospital, Alkhobar, College of Medicine, Imam Abdulrahman bin Faisal University, Dammam, Kingdom of Saudi Arabia
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Article Figures & Data

Figures

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  • Figure 1
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    Figure 1

    - Clinical presentations and characteristics of lesions suspicious of MF. (A) Patches present for > 6 months in the upper arm and trunk that were associated with hypopigmentation; the lesions were suspicious of MF. (B) Multiple erythematous papules, accompanied by intense pruritus of the upper arms and H&E-confirmed MF diagnosis. (C) Multiple hyperpigmented scaly patches involving the trunk and H&E-confirmed MF diagnosis. (D) Clinical characteristics of lesions suspicious of MF and their presence in MF cases (n=34) and non-MF cases (n=22). The graph shows that erythema and itching were significantly more common in MF cases than in non-MF cases. H&E: hematoxylin and eosin staining, MF: mycosis fungoides

  • Figure 2
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    Figure 2

    - Histological features used in the study to distinguish mycosis fungoides (MF) from non-MF cases. A) Epidermotropism is significantly found in MF cases compared with non-MF cases. B) Spongiosis (Grade 1) is present in MF cases, where it is located at the epidermal sites invaded by atypical lymphocytes (black rectangle). Areas not invaded by atypical lymphocytes show no spongiosis (black arrow). C) Pautrier’s microabscesses are significantly found more in the plaque stage than in the patch stage of MF (original, ´200 all).

  • Figure 3
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    Figure 3

    - Immunohistochemical staining of mycosis fungoides cases. A) Positive expression of pan T-cell markers (CD3). B) Positive expression of CD4. C) Positive expression of CD8 with a ratio of 2.5:1 epidermally. D) Positive expression of CD5. (E) Loss of CD7. (original, ´200 all)

Tables

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    Table 1

    - Grading of histological parameters for the assessment of suspected mycosis fungoides.

    Histological criteriaGrade 0Grade 1Grade 2Grade 3
    Epidermotropism(-)Focal (1-5/HPF)Moderate (6-10/HPF)Marked (> 10/HPF)
    Pautrier’s microabscess(-)(+)NANA
    Spongiosis*(-)Mild (focal)ModerateSevere
    Parakeratosis(-)Focal (<10%)Moderate (10-50%)Marked (>50%)
    Pigment incontinence(-)(+)NANA
    Dermal infiltrates(-)Mild perivascularLichenoid patternDense with adnexal structure
    Dermal fibrosis(-)(+)NANA
    Atypical lymphocytes(-)1–5/100 cells6–10/100 cells>10/100 cells
    Large cerebriform lymphocytes(-)1–3/10 HPF4–5/10 HPF>5/100 HPF
    Adnexal involvement(-)(+)NANA

    HPF: high-power field, NA: not applicable

    • ↵* Spongiosis was assessed as follows: mild=degree of intercellular edema mildly greater than what would be typically expected for the interface change displayed within the specimen, moderate=moderate spongiotic change, severe=severe spongiotic change with vesicle or bullae formation.

    • View popup
    Table 2

    - Profile of 56 patients included in the study.

    Number of patients (N=56)Clinical presentation of the patientsLesions with hypopigmentation (n)Lesions with hyperpigmentation (n)Lesions with erythema (n)Lesions with scales (n)Association with itching (n)
    4Macules13011
    20Patches431495
    22Plaques06212114
    4Nodules00300
    2Follicular eruption01111
    2Erythroderma00220
    2Poikiloderma20200
    Number of patients (N=56)Association with lymphadenopathy (n)Confirmed MF cases (n)Diagnosis of non-MF cases (n)Average age of patients diagnosed with MF (years)Female-to-male ratio in MF cases
    400LP (1); PA (1); Inconclusive(1); PIH (1)00
    20011PA (1); DE (1); TC (2); Psoriasis (1); Inconclusive(4)525:6
    22014Psoriasis (3) SD (1); DE (1); TC (1); Inconclusive(2)574:10
    444-593:1
    201LP (1)451:0
    222-700:2
    202-390:2

    MF: mycosis fungoides, n: number of cases, PIH: post inflammatory hyperpigmentation, LP: lichen planus, PA: pityriasis alba, DE: discoid eczema, SD: statis dermatitis, TC; tinea corporis

      • View popup
      Appendix 1

      - Histological feature analysis of the 56 suspected mycosis fungoides (MF) lesions involved in the study.

      Case no.DiagnosisClinical featureEpidermotropismEpidermotropism grade *Pautrier’s microabscessSpongiosisSpongiosis gradeParakeratosis
      1MFpatch111111
      2MFpatch111111
      3MFpatch110111
      4MFpatch110111
      5MFpatch110110
      6MFpatch110110
      7MFpatch120111
      8MFpatch121111
      9MFpatch000110
      10MFpatch000111
      11MFpatch000111
      12MFplaque001121
      13MFplaque111111
      14MFplaque111111
      15MFplaque111111
      16MFplaque111111
      17MFplaque111111
      18MFplaque110110
      19MFplaque110110
      20MFplaque110110
      21MFplaque121111
      22MFplaque121111
      23MFplaque121121
      24MFplaque110111
      25MFplaque111001
      26MFnodule111111
      27MFnodule111000
      28MFnodule000110
      29MFnodule000000
      30MFerythroderma110111
      31MFerythroderma000111
      32MFpoikiloderma110110
      33MFpoikiloderma000000
      34MFfollicular111110
      35non-MFpatch000000
      36non-MFpatch000111
      37non-MFpatch000111
      38non-MFpatch000110
      39non-MFpatch000110
      40non-MFpatch000110
      41non-MFpatch000110
      42non-MFpatch000110
      43non-MFpatch000120
      44non-MFplaque000111
      45non-MFplaque000111
      46non-MFplaque000111
      47non-MFplaque000110
      48non-MFplaque000110
      49non-MFplaque000120
      50non-MFplaque000000
      51non-MFplaque000110
      52non-MFfollicular000110
      53non-MFmacule000000
      54non-MFmacule000000
      55non-MFmacule000000
      56non-MFmacule000000
      Case no.Parakeratosis gradeAtypical lymphocytesAtypical lymphocytes gradeCerebriform lymphocytesCerebriform lymphocytes gradeInfiltrating lymphocytesInfiltration gradePigment incontinenceAdnexal involvementDermal fibrosis
      11111111101
      21111211101
      31111111001
      41111111001
      50000011001
      60000011000
      72121212001
      81121211001
      90111112000
      101000011000
      111000011000
      121000011000
      131000011000
      141000011000
      151000011000
      161000011000
      171111111001
      180111111000
      190111112000
      200111212000
      211000011000
      222111111001
      232121312001
      241111111000
      251000012101
      261121213111
      270121212001
      280121212000
      290121212000
      301111112101
      311111112001
      320111111101
      330111111101
      340111112101
      350000011000
      360000012100
      370000012100
      380000011000
      390000011000
      400000011000
      410000011000
      420000011000
      430000011000
      441000011000
      451000011100
      461000011100
      470000011000
      480000011000
      490000011000
      500000011000
      510000011000
      520000011000
      530000011000
      540000011000
      550000011000
      560000011000
      • ↵* Traits were graded from 0 to 3 in epidermotropism, spongiosis, parakeratosis, dermal infiltrate, atypical lymphocytes, and large atypical cerebriform cells and graded from 0 to 1 in Pautrier’s microabscess, pigment incontinence, dermal fibrosis, and adnexal involvement. Analysis was performed using Fisher’s exact test with a Bonferroni-corrected threshold of significance = 0.005 = 0.05/10). If a significant association found, follow-up testing was performed to assess the grade severity of a trait vis-à-vis the diagnosis, using ordinal logistic regression (using maximum likelihood fitting), in 2 ways: first, by including zero values in the response variable (0, 1, 2, 3; 5 models fitted), and second, by considering only non-zero cases (such as including only those patients exhibiting the trait). When narrowing the testing to the patch and plaque groups only, 2×2 contingency tables (Fisher’s exact test, 2-tailed) were used. Likewise, it is pertinent to know whether the grade severity of a trait differentiating MF from a non-MF diagnosis was also more pronounced in patch versus plaque patients. To this end, non-zero cases were excised, and contingency tables were analysed (9 2×2 tables with Fisher’s exact test and one 3×2 table analysed with a likelihood ratio test of the chi-square). Finally, for either the patch or plaque subgroup, 10 goodness-of-fit tests were performed, 1 per histological trait, to determine where the observed counts of presence/absence deviated from those expected by chance (such as 50% frequency of occurrence).

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    Differentiating mycosis fungoides lesions from their mimickers clinically and histologically
    Fatimah M. Budair, Ahmed A. Alsayyah, Omar M. Alakloby
    Saudi Medical Journal Dec 2024, 45 (12) 1355-1367; DOI: 10.15537/smj.2024.45.12.20240796

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    Differentiating mycosis fungoides lesions from their mimickers clinically and histologically
    Fatimah M. Budair, Ahmed A. Alsayyah, Omar M. Alakloby
    Saudi Medical Journal Dec 2024, 45 (12) 1355-1367; DOI: 10.15537/smj.2024.45.12.20240796
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    Keywords

    • mycosis fungoides
    • immunohistochemistry
    • dermatology
    • histopathology

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