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Jessner lymphocytic infiltrate of the skin is a cutaneous condition characterized by a persistent papular and plaque-like skin eruption which can occur on the neck, face and back and may re-occur. This is an uncommon skin disease and is a benign collection of lymph cells. Its cause is not known and can be hereditary.
Lymphoid hyperplasia is the rapid proliferation of normal lymphocytic cells that resemble lymph tissue which may occur with bacterial or viral infections. [1] The growth is termed hyperplasia which may result in enlargement of various tissue including an organ, or cause a cutaneous lesion .
Lymphoproliferative disorders (LPDs) refer to a specific class of diagnoses, comprising a group of several conditions, in which lymphocytes are produced in excessive quantities. These disorders primarily present in patients who have a compromised immune system .
Cutaneous B-cell lymphomas (CBCL), more recently termed Primary cutaneous B-cell lymphomas and lymphoproliferative disorders (PCBCLPD), are a group of disorders that typically present as skin lesions consisting of proliferating B-cells. B-cells are a type of lymphocyte involved in regulating immune responses.
Lymphadenopathies such as follicular hyperplasia can show various symptoms such as fever, chills, night sweats, unexplained weight loss and prominent localizing symptoms are non age and non-gender specific. [4] Although human lymph nodes cannot be seen with the naked eye, if you press against the skin you can sometimes feel for swelling and ...
Nodular pattern of cutaneous lymphoid hyperplasia; Non-mycosis fungoides CD30− cutaneous large T-cell lymphoma; Non-mycosis fungoides CD30− pleomorphic small/medium sized cutaneous T-cell lymphoma; Non-mycosis fungoides CD30- pleomorphic small/medium sized cutaneous T-cell lymphoma; Nonspecific cutaneous conditions associated with leukemia
Similar to cutaneous anaplastic large-cell lymphoma, with larger clusters or sheets of large anaplastic CD30+ cells without the interspersed mixed infiltrate of Type A. D Similar to CD8+ epidermotropic cutaneous T-cell lymphoma , with large CD8 + and CD30+ lymphocytes that often stain with cytotoxic markers (TIA-1, granzyme, perforin).
Historically, bilateral parotid and lacrimal gland enlargement was characterized by the term Mikulicz's disease if the enlargement appeared apart from other diseases. If it was secondary to another disease, such as tuberculosis, sarcoidosis, lymphoma, and Sjögren's syndrome, the term used was Mikulicz's syndrome.