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DERMATOPHYTOSIS INCOGNITO MIMICKING CUTANEOUS T-CELL LYMPHOMA

Shahab Babakoohi • Chad M. McCall



Shahab Babakoohi • Chad M. McCall

Published: June 10, 2022

DOI: 10.7759/cureus.25809

Cite this article as: Babakoohi S, McCall C M (June 10, 2022) Dermatophytosis
Incognito Mimicking Cutaneous T-Cell Lymphoma. Cureus 14(6): e25809.
doi:10.7759/cureus.25809


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ABSTRACT

Dermatophytosis incognito can be missed in diagnosis, given its relatively low
prevalence as compared with common cases of dermatophytosis and therefore, is
likely under-reported. Cutaneous T-cell lymphoma (CTCL) is also a rare entity
with variable clinical manifestations. While successful treatment of
dermatophytosis is feasible with multiple topical and systemic antifungal
options, CTCL can present a therapeutic challenge associated with significant
emotional distress for the patients. We present a case of tinea incognito
initially treated for eczema, later considered biopsy-supported CTCL that was
successfully treated with antifungal therapy.


INTRODUCTION

Dermatophytosis incognito is a condition seen in an untreated fungal
infection following the application of topical corticosteroids which may not
always manifest with typical tinea symptoms [1]. It is often inadvertently
treated as inflammatory dermatoses such as eczema prior to the correct
diagnosis. Cutaneous T-cell lymphoma (CTCL) includes a broad spectrum of
subtypes and clinical manifestations of cutaneous malignant clonal T
lymphocytes. Mycosis fungoides is the most common type [2]. CTCL can also be
misdiagnosed and treated as inflammatory dermatoses. Despite significant
diagnostic advances including cultures, special stains, and molecular pathology
in the diagnosis of these entities, clinical suspicion still plays a major role.


CASE PRESENTATION

The patient was a 62-year-old woman with a history of chronic myeloid leukemia
and polycythemia vera with myelofibrosis diagnosed in 2009; she went into
remission after a hematopoietic stem cell transplant in 2015. In 2020, she
developed a pruritic rash on the right shin with a large plaque and a small rash
on the right elbow (Figure 1). She was diagnosed with eczema and treated
with multiple lines of potent topical corticosteroids for greater than six
months. The rash, inflammation, and pruritus progressively worsened. She was
referred to oncologic dermatology.

FIGURE 1: A. RIGHT SHIN ERUPTION AT PRESENTATION; B. AFTER ONE MONTH OF
TERBINAFINE




With a clinical impression of dermatophytosis incognito, empiric ketoconazole
cream was started. Systemic treatment was deferred pending the results of
pathology, microbiology tissue cultures, and evaluation of response to topical
therapy.

Histopathology of the punch biopsy from the right shin showed an atypical
lymphoid infiltrate with small lymphocytes with irregular nuclear contours and
clear cytoplasm, which was centered in the dermis with focal evidence of
epidermotropism (Figure 2). The infiltrate extended around the adnexal
structures and blood vessels and had focal involvement of the hair follicle. A
periodic acid-Schiff (PAS) stain was negative for fungal elements. The atypical
lymphocytes were positive for CD3 and CD4 with partial loss of CD7 expression.
CD8 highlighted background T cells. CD30 was positive in very rare cells. CD20
highlighted very rare background B cells. The findings were compatible with a
diagnosis of mycosis fungoides. 

FIGURE 2: A. DERMAL-BASED LYMPHOID INFILTRATE WITH FOCAL EVIDENCE OF
EPIDERMOTROPISM (H&E, 200X). B. EPIDERMAL LYMPHOCYTES WITH IRREGULAR NUCLEAR
CONTOURS AND CLEAR CYTOPLASM (ARROWS) (H&E, 400X). C. CD3 IMMUNOHISTOCHEMICAL
STAIN HIGHLIGHTING T-CELLS, WHICH ACCOUNT FOR MOST OF THE LYMPHOID INFILTRATE
(200X). D. CD4 IMMUNOHISTOCHEMICAL STAIN HIGHLIGHTING THE MAJORITY OF THE
T-CELLS, AS WELL AS DIMLY STAINING DENDRITIC CELLS AND MACROPHAGES (200X). E.
CD7 IMMUNOHISTOCHEMICAL STAIN SHOWING PARTIAL LOSS OF EXPRESSION IN THE T-CELLS
(200X). F. CD8 IMMUNOHISTOCHEMICAL STAIN SHOWING BACKGROUND CYTOTOXIC T-CELLS,
FEWER IN NUMBER THAN CD4-POSITIVE CELLS (200X).




A preliminary discussion was performed with the patient for potential treatment
options including both topical and systemic CTCL therapies given the failure of
topical corticosteroid treatment. Given the extensive history of hematologic
malignancies with complications of systemic treatments, she was unwilling to
proceed with systemic agents in case of failure of topical options.

During ongoing discussions regarding CTCL treatment, the patient reported a
notable improvement in inflammation of rash after several days of ketoconazole
cream application, thrice daily. Prior to the consideration of mycosis
fungoides-directed therapy, an oral terbinafine course was tried. T-cell
receptor gamma gene rearrangement assay returned negative for monoclonality
while receiving oral antifungal agent.

The patient reported significant improvement one week after treatment. The right
elbow rash resolved after two weeks of treatment. One month after treatment, the
right shin plaque had dramatically improved.

Tissue culture for bacterial, fungal, and atypical mycobacterial infection
remained negative. The patient did not return for further follow-up as she
reported complete resolution. 


DISCUSSION

Dermatophytosis incognito is seen in untreated superficial fungal
infections treated with corticosteroids. PAS staining sensitivity varies in the
literature from 70% to 98% [3]. A negative result does not confidently exclude
the diagnosis. There are few studies on the sensitivity of tissue culture for
dermatophytes. In one study, clinical assessment was used as the gold standard
for tinea pedis. The sensitivities for KOH smear and culture were approximately
73% and 42%, respectively [4].

CTCL, a lymphoma that is generally known as a liquid tumor, has a predilection
for the skin. While it is frequently limited to the skin, it can spread into the
lymphatic system and even enter the leukemic phase known as Sezary syndrome [5].
CTCL is diagnosed by histopathology features, immunohistochemistry, and
molecular markers. In histopathology, diffuse dermal infiltrate of neoplastic
T-cells is seen [6]. Among immunophenotypical characteristics, the most common
finding is loss of CD7 expression; however, CD7 expression loss can be a
reactive phenomenon and has been reported in inflammatory benign dermatosis [7].
Accumulation of CD7 negative T-cell lymphocytes has been reported in lymphocytic
infiltrates and inflammatory skin lesions [8] Our patient did regularly shave
her legs which is a known risk factor for dermatophytosis infection in the
setting of immunosuppression. Her right elbow rash could be an
autoeczematization reaction which resolved simultaneously with the improvement
of leg eruption.


CONCLUSIONS

Mycosis fungoides and dermatophytosis incognito can have overlapping features.
Histopathology, special stains, or culture may not clearly differentiate these
two entities. Clinicians need to use their clinical skills in the diagnosis of
complex dermatoses, especially when some treatment options would be prolonged,
aggressive, or bear considerable side effects.


REFERENCES

 1. Seitz AT, Paasch U, Simon JC, Ziemer M: Tinea incognito. J Dtsch Dermatol
    Ges. 2013, 11:1090-3. 10.1111/ddg.12156
 2. Koh HK, Charif M, Weinstock MA: Epidemiology and clinical manifestations of
    cutaneous T-cell lymphoma. Hematol Oncol Clin North Am. 1995, 9:943-60.
 3. Shalin SC, Ferringer T, Cassarino DS: PAS and GMS utility in
    dermatopathology: review of the current medical literature. J Cutan Pathol.
    2020, 47:1096-102. 10.1111/cup.13769
 4. Levitt JO, Levitt BH, Akhavan A, Yanofsky H: The sensitivity and specificity
    of potassium hydroxide smear and fungal culture relative to clinical
    assessment in the evaluation of tinea pedis: a pooled analysis. Dermatol Res
    Pract. 2010, 2010:764843. 10.1155/2010/764843
 5. Hamad H, Mangla A: Lymphocytosis. StatPearls Publishing, Treasure Island
    (FL); 2022. https://pubmed.ncbi.nlm.nih.gov/31747226/.
 6. Willemze R: Primary cutaneous lymphoma: the 2018 update of the WHO-EORTC
    classification. Presse Med. 2022, 51:104126. 10.1016/j.lpm.2022.104126
 7. Murphy M, Fullen D, Carlson JA: Low CD7 expression in benign and malignant
    cutaneous lymphocytic infiltrates: experience with an antibody reactive with
    paraffin-embedded tissue. Am J Dermatopathol. 2002, 24:6-16.
    10.1097/00000372-200202000-00002
 8. Moll M, Reinhold U, Kukel S, Abken H, Müller R, Oltermann I, Kreysel HW:
    CD7-negative helper T cells accumulate in inflammatory skin lesions. J
    Invest Dermatol. 1994, 102:328-32.

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