皮膚リンパ球腫
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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2015/09/23 21:48:57」(JST)
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| Cutaneous lymphoid hyperplasia |
|
borrelial lymphocytoma on the cheek
|
| Classification and external resources |
| Specialty |
dermatology |
| ICD-10 |
L98.8 (ILDS L98.812) |
| MeSH |
D019310 |
Cutaneous lymphoid hyperplasia (also known as "borrelial lymphocytoma,"[1] "Lymphadenosis benigna cutis," "Lymphocytoma cutis," "Pseudolymphoma," "Pseudolymphoma of Spiegler and Fendt,"[1] "Sarcoidosis of Spiegler and Fendt,"[1] "Spiegler–Fendt lymphoid hyperplasia,"[1] and "Spiegler–Fendt sarcoid") refers to a groups of benign cutaneous disorders characterized by collections of lymphocytes, macrophages, and dendritic cells in the skin.[2]:725 Conditions included in this groups are:[2]:725
- Cutaneous lymphoid hyperplasia with nodular pattern, a condition of the skin characterized by a solitary or localized cluster of asymptomatic erythematous to violaceous papules or nodules.[2]:725
- Cutaneous lymphoid hyperplasia with bandlike and perivascular patterns, a condition of the skin characterized by skin lesions that clinically resemble mycosis fungoides.[2]:726
| Jessner lymphocytic infiltrate of the skin |
| Classification and external resources |
| Specialty |
dermatology |
| DiseasesDB |
33040 |
| eMedicine |
article/1098654 |
- Jessner lymphocytic infiltrate of the skin (also known as "Benign lymphocytic infiltration of the skin,"[1] "Jessner lymphocytic infiltration of the skin," "Jessner–Kanof lymphocytic infiltration of the skin," and "Lymphocytic infiltrate of Jessner") 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. The cause of this is not known and can be hereditary.[1]:1887[2]:727 It is named for Max Jessner.[3][4] It has been suggested that it is equivalent to lupus erythematosus tumidus.[5]
See also
- Skin lesion
- List of cutaneous conditions
References
- ^ a b c d e f Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 1-4160-2999-0.
- ^ a b c d e James, William D.; Berger, Timothy G. et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 0-7216-2921-0.
- ^ synd/1371 at Who Named It?
- ^ ORFUSS AJ (October 1953). "Lymphocytic infiltration of the skin". AMA Arch Derm Syphilol 68 (4): 447–9. PMID 13091384.
- ^ Jessner Lymphocytic Infiltration of the Skin at eMedicine
|
Hematological malignancy/leukemia histology (ICD-O 9590–9989, C81–C96, 200–208)
Lymphoid/Lymphoproliferative, Lymphomas/Lymphoid leukemias (9590–9739, 9800–9839)
|
|
B cell
(lymphoma,
leukemia)
(most CD19
|
By development/
marker |
| TdT+ |
- ALL (Precursor B acute lymphoblastic leukemia/lymphoma)
|
|
| CD5+ |
- mantle zone (Mantle cell)
|
|
| CD22+ |
- Prolymphocytic
- CD11c+ (Hairy cell leukemia)
|
|
| CD79a+ |
- germinal center/follicular B cell (Follicular
- Burkitt's
- GCB DLBCL
- Primary cutaneous follicular lymphoma)
- marginal zone/marginal-zone B cell (Splenic marginal zone
- MALT
- Nodal marginal zone
- Primary cutaneous marginal zone lymphoma)
|
|
| RS (CD15+, CD30+) |
- Classic Hodgkin's lymphoma (Nodular sclerosis)
- CD20+ (Nodular lymphocyte predominant Hodgkin's lymphoma)
|
|
PCDs/PP
(CD38+/CD138+) |
- see immunoproliferative immunoglobulin disorders
|
|
|
| By infection |
- KSHV (Primary effusion)
- EBV (Lymphomatoid granulomatosis
- Post-transplant lymphoproliferative disorder)
- HIV (AIDS-related lymphoma)
- Helicobacter pylori (MALT lymphoma)
|
|
| Cutaneous |
- Diffuse large B-cell lymphoma
- Intravascular large B-cell lymphoma
- Primary cutaneous marginal zone lymphoma
- Primary cutaneous immunocytoma
- Plasmacytoma
- Plasmacytosis
- Primary cutaneous follicular lymphoma
|
|
|
| T/NK |
T cell
(lymphoma,
leukemia)
(most CD3
|
By development/
marker |
- TdT+: ALL (Precursor T acute lymphoblastic leukemia/lymphoma)
- prolymphocyte (Prolymphocytic)
- CD30+ (Anaplastic large-cell lymphoma
- Lymphomatoid papulosis type A)
|
|
| Cutaneous |
| MF+variants |
- indolent: Mycosis fungoides
- Pagetoid reticulosis
- Granulomatous slack skin
aggressive: Sézary disease
- Adult T-cell leukemia/lymphoma
|
|
| Non-MF |
- CD30-: Non-mycosis fungoides CD30− cutaneous large T-cell lymphoma
- Pleomorphic T-cell lymphoma
- Lymphomatoid papulosis type B
- CD30+: CD30+ cutaneous T-cell lymphoma
- Secondary cutaneous CD30+ large cell lymphoma
- Lymphomatoid papulosis type A
|
|
|
| Other peripheral |
- Hepatosplenic
- Angioimmunoblastic
- Enteropathy-associated T-cell lymphoma
- Peripheral T-cell lymphoma-Not-Otherwise-Specified (Lennert lymphoma)
- Subcutaneous T-cell lymphoma
|
|
| By infection |
- HTLV-1 (Adult T-cell leukemia/lymphoma)
|
|
|
NK cell/
(most CD56) |
- Aggressive NK-cell leukemia
- Blastic NK cell lymphoma
|
|
| T or NK |
- EBV (Extranodal NK-T-cell lymphoma/Angiocentric lymphoma)
- Large granular lymphocytic leukemia
|
|
|
| Lymphoid+myeloid |
- Acute biphenotypic leukaemia
|
|
| Lymphocytosis |
- Lymphoproliferative disorders (X-linked lymphoproliferative disease
- Autoimmune lymphoproliferative syndrome)
- Leukemoid reaction
- Diffuse infiltrative lymphocytosis syndrome
|
|
|
| Cutaneous lymphoid hyperplasia |
- Cutaneous lymphoid hyperplasia
- with bandlike and perivascular patterns
- with nodular pattern
- Jessner lymphocytic infiltrate of the skin
|
|
|
Index of the immune system
|
|
| Description |
- Physiology
- cells
- autoantigens
- autoantibodies
- complement
- surface antigens
- IG receptors
|
|
| Disease |
- Allergies
- Immunodeficiency
- Immunoproliferative immunoglobulin disorders
- Hypersensitivity and autoimmune disorders
- Neoplasms and cancer
|
|
| Treatment |
- Procedures
- Drugs
- antihistamines
- immunostimulants
- immunosuppressants
- monoclonal antibodies
|
|
|
UpToDate Contents
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English Journal
- Lymphocytoma cutis--case report.
- Oliveira EV, Badiale GB1, Moraes MM2.
- Anais brasileiros de dermatologia.An Bras Dermatol.2013 Nov-Dec;88(6 Suppl 1):128-31. doi: 10.1590/abd1806-4841.20132320.
- We describe a clinical case involving a 62-year-old white male, diagnosed with lymphocytoma cutis (Spiegler-Fendt sarcoid) in the cephalic segment. The diagnosis was carried out by pathological study and confirmed by immunohistochemical panel: evidence of polyclonality. Phototherapy sessions were su
- PMID 24346899
- [B-pseudolymphoma: lymphocytoma].
- Torres Cortijo A, Ortíz Medina A.
- Medicina cutánea ibero-latino-americana.Med Cutan Ibero Lat Am.1986;14(6):371-86.
- We have revised the concept of pseudolymphoma, some of its classifications and its differences with the malignant lymphoma, which sometimes are only an evolution, not existing other elements of judgement. We publish the summary of ten lymphocytoma cutis cases studied by us, which we believe are the
- PMID 3550311
- [Spiegler-Fendt sarcoid].
- Furmaniuk J, Owczarek L.
- Polski tygodnik lekarski (Warsaw, Poland : 1960).Pol Tyg Lek.1971 Dec 20;26(51):1990-1.
- PMID 5139582
Japanese Journal
- Brill-Symmers病,Spiegler-Fendt sarcoidおよび著者等の経験せる"リンパ濾胞様構造および好酸球増多を示す一種の肉芽腫"の3症例について
Related Links
- Information about Spiegler-Fendt sarcoid in Free online English dictionary. What is Spiegler-Fendt sarcoid? Meaning of Spiegler-Fendt sarcoid medical term. What does Spiegler-Fendt sarcoid mean? Spiegler-Fendt sarcoid ? ...
- Spiegler-Fendt sarcoid symptoms, causes, diagnosis, and treatment information for Spiegler-Fendt sarcoid (Bäfverstedt syndrome) with alternative diagnoses, full-text book chapters, misdiagnosis, research treatments, prevention, and ...
★リンクテーブル★
[★]
- 英
- lymphocytoma cutis
- 同
- 皮膚良性リンパ腺腫症 皮膚良性リンパ節症 lymphadenosis benigna cutis、シュピーグラー・フェント類肉腫 Spiegler-Fendt sarcoid
- 関
- 皮膚リンパ球腫
[★]
- 関
- eruption、skin eruption、skin rash