B-cell lymphoma of the skin: clinical observation

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Abstract

Currently, there is an increase and an increase in the incidence of primary skin lymphomas worldwide. B-cell cutaneous lymphomas account for 25–30% of primary skin lymphomas. Among all skin lymphomas, primary cutaneous lymphoma from follicular center cells occurs in 10–11% of cases and is characterized by great diagnostic difficulties due to the great similarity of clinical manifestations with other dermatoses, such as benign lymphoplasia, Beck's sarcoidosis, Jessner–Kanof lymphocytic infiltration, skin metastases.

This paper presents a clinical case of B-cell lymphoma in a 29-year-old woman with a lesion of the facial skin in the form of a node, initially incorrectly interpreted as benign lymphoplasia. For five years, the patient received therapy with topical glucocorticosteroids with no effect from. Subsequently, histological examination and immunohistochemistry were performed for the purpose of differential diagnosis of sarcoidosis with B-cell lymphoma. Histologically, there is nodular proliferation of atypical lymphoid cells in the dermis, most of which have cytological characteristics of a centrocyte with an admixture of a small number of central blasts. Nodular proliferates contain an admixture of compactly arranged small lymphocytes. There are no signs of epidermotropism. During immunohistochemical examination, cells forming nodular proliferates express CD20, bc16 with an index of proliferative activity for the expression of nuclear protein K167 ― 20–30%, a dissociated network of follicular dentritic cells expressing CD21 is determined at the base of nodular proliferates. They are not expressed by bc12, CD3, CD2, CD5 proliferate cells. CD117 is expressed by an admixture of discretely distributed mast cells. The morphological picture corresponds to primary cutaneous centrofollicular lymphoma. The node was excised. Radiation therapy was not prescribed due to the patient's pregnancy.

This clinical observation highlights the importance of considering the diagnosis of lymphoma in the differential diagnosis of treatment-resistant dermatological diseases.

About the authors

Yulia V. Karacheva

Professor V.F. Voino-Yasenetsky Krasnoyarsk State Medical University

Email: julkar19@yandex.ru
ORCID iD: 0000-0002-7025-6824
SPIN-code: 4789-9178

MD, Dr. Sci. (Med.), Associate Professor

Russian Federation, Krasnoyarsk

Anastasia N. Smykova

Professor V.F. Voino-Yasenetsky Krasnoyarsk State Medical University

Author for correspondence.
Email: smykova.a@mail.ru
ORCID iD: 0000-0001-5846-4244
SPIN-code: 2226-9685

MD, Cand. Sci. (Med.)

Russian Federation, Krasnoyarsk

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Supplementary files

Supplementary Files
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1. JATS XML
2. Fig. 1. Patient P., 29 years old. A horseshoe-shaped burgundy-red nodule of 3×2 cm in size, painless, dense-elastic consistency, with a smooth surface was located on the skin of the forehead on the left side.

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3. Fig. 2. Results of histological and immunohistochemical examination: a ― overview view of skin preparation with nodular proliferate tumour lymphoid cells; b ― predominantly centrocytic composition of nodular tumour proliferates with admixture of a small number of centroblasts; c ― nuclear expression of bcl6 by tumour cells; d ― dislocated network of follicular dendritic cells expressing CD23 at the base of tumour proliferates; e ― nuclear expression of LMO2 by tumour cells; f ― tumour cells do not express bcl2; g ― expression of CD20 by tumour cells; h ― expression of Ki67 nuclear protein by tumour cells.

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4. Fig. 3. Postoperative scar on the forehead skin as a result of tumour excision.

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