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. 2025 Jul-Aug;100(4):501133.
doi: 10.1016/j.abd.2025.501133. Epub 2025 Jun 18.

Rare case of lymphomatoid papulosis type E

Máté Attila Bognár  1 , Csaba Gyömörei  2 , Zsuzsanna Lengyel  3
Affiliations

Rare case of lymphomatoid papulosis type E

Máté Attila Bognár et al. An Bras Dermatol. 2025 Jul-Aug.
No abstract available

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Conflict of interest statement

Conflicts of interest None declared.

Figures

Figure 1
Figure 1
Erythematous papulonodular lesions (A) progressing into necrotic ulcers (B).
Figure 2
Figure 2
Low-power view showing epidermal ulceration and a dermal-based angiocentric lymphocytic infiltrate (Hematoxylin & eosin, original magnification 15×) (A). High-power image showing an angiodestructive medium-sized, to large-sized atypical lymphocytic infiltrate (Hematoxylin & eosin, original magnification 400×) (B). The tumor cells were extensively immunoreactive for CD3 (C) and CD30 (D) (CD3 and CD30 immunostain, original magnification 384× and 279×).
Figure 3
Figure 3
Extensive ulceration and necrosis of the lesions (A‒B).
See this image and copyright information in PMC

References

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