Cutaneous borreliosis associated with T cell–predominant infiltrates: A diagnostic challenge  

Oleh:

Kempf, Werner ; Kazakov, Dmitry V. ; Hubscher, Eugen ; Gugerli, Oliver

Jenis: Article from Journal - ilmiah internasional
Dalam koleksi: JAAD: Journal of the American Academy of Dermatology (keterangan: ada di ClinicalKey) vol. 72 no. 04 (Apr. 2015), page 683-689.
Topik: borreliosis; cutaneous T-cell lymphoma; interstitial granulomatous dermatitis; T cell

Ketersediaan

Perpustakaan FK Nomor Panggil: J15.K Non-tandon: 1 (dapat dipinjam: 0) Tandon: tidak ada

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Isi artikel

Background With the exception of erythema migrans, Borrelia infection of the skin manifests much more commonly with B cell–rich infiltrates. T cell–rich lesions have rarely been described. Objective We report a series of 6 patients with cutaneous borreliosis presenting with T cell–predominant skin infiltrates. Methods We studied the clinicopathologic and molecular features of 6 patients with T cell–rich skin infiltrates. Results Half of the patients had erythematous patchy, partly annular lesions, and the other patients had features of acrodermatitis chronica atrophicans. Histopathology revealed a dense, band-like or diffuse dermal infiltrate. Apart from small, well differentiated lymphocytes, there were medium-sized lymphocytes with slight nuclear atypia and focal epidermotropism. An interstitial histiocytic component was found in 4 cases, including histiocytic pseudorosettes. Fibrosis was present in all cases but varied in severity and distribution. In 5 patients, borrelia DNA was detected in lesional tissue using polymerase chain reaction studies. No monoclonal rearrangement of T-cell receptor gamma genes was found. Limitations This retrospective study was limited by the small number of patients. Conclusion In addition to unusual clinical presentation, cutaneous borreliosis can histopathologically manifest with a T cell–rich infiltrate mimicking cutaneous T-cell lymphoma. Awareness of this clinicopathologic constellation is important to prevent underrecognition of this rare and unusual presentation representing a Borrelia-associated T-cell pseudolymphoma.

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