ライフサイエンスコーパス: lymphoplasmacytic

1 tion is associated with moderate, multifocal lymphoplasmacytic ampullitis comprising clusters of B (C

2 erized by expansion of the lamina propria by lymphoplasmacytic and histiocytic infiltrates.

3 of mice is affected by AIH, characterized by lymphoplasmacytic and periportal hepatic infiltrates, au

4 A significant fraction of thoracic lymphoplasmacytic aortitis cases, about 40% of inflammat

5 immune pancreatitis, sclerosing cholangitis, lymphoplasmacytic aortitis, salivary gland involvement,

6 ma characterized by elevated serum IgM and a lymphoplasmacytic bone marrow infiltrate.

7 ortem lung examination of sibling 2 revealed lymphoplasmacytic bronchiolitis with intraluminal purule

8 variation in disease progression, including lymphoplasmacytic bronchiolitis, BOOP, and death.

9 least in part to the presence of a prominent lymphoplasmacytic cell infiltrate in the tumor stroma, w

10 east in part, to the presence of a prominent lymphoplasmacytic cell infiltrate in the tumor stroma.

11 We studied the B lymphoplasmacytic cell infiltrates in MCB to determine t

12 pathy and bone marrow (BM) infiltration with lymphoplasmacytic cells (LPCs).

13 posed of both small B lymphocytes and larger lymphoplasmacytic cells and plasma cells: CD3(-), CD19(+

14 Tumor-infiltrating lymphoplasmacytic cells are a key feature of medullary c

15 dy response produced by tumor-infiltrating B lymphoplasmacytic cells are autoimmune in nature and a c

16 terface hepatitis; (2) acidophil bodies with lymphoplasmacytic cells are seen in early recurrent AIH;

17 We genotyped lymphoplasmacytic cells from 175 WM patients and observe

18 We sequenced sorted CD19(+) lymphoplasmacytic cells from 6 WM patients who progresse

19 k factors for progression were percentage of lymphoplasmacytic cells in the bone marrow, size of the

20 isorder characterized by the infiltration of lymphoplasmacytic cells into bone marrow and the presenc

21 ainst actin produced by tumor-infiltrating B lymphoplasmacytic cells is Ag-driven, affinity-matured,

22 braries were generated from MCB-infiltrating lymphoplasmacytic cells of two patients, and MCB-reactiv

23 levels raises issues on interactions between lymphoplasmacytic cells, mast cells, and endothelial cel

24 ion of clonal immunoglobulin (Ig)M-secreting lymphoplasmacytic cells.

25 ne marrow, of clonally related IgM-secreting lymphoplasmacytic cells.

26 one marrow (BM) involvement of IgM secreting lymphoplasmacytic cells.

27 with CD20+, IgM+, and monotypic light chain+ lymphoplasmacytic cells.

28 otubules and with clinical associations with lymphoplasmacytic disorders.

29 phoid neoplasm characterised by a monoclonal lymphoplasmacytic expansion accompanied by a serum monoc

30 tion of the main stomach revealed multifocal lymphoplasmacytic gastritis with silver-stained spiral-s

31 Multifocal lymphoplasmacytic hepatitis was observed in 9 of 17, 15

32 ed with wild type exhibited moderate lobular lymphoplasmacytic hepatitis with hepatocytic coagulative

33 rane by electron microscopy and a pronounced lymphoplasmacytic infiltrate by histologic examination.

34 IgG4-RD is characterized by a lymphoplasmacytic infiltrate composed of IgG4(+) plasma

35 ated disease (IgG4-RD) is characterized by a lymphoplasmacytic infiltrate composed of IgG4(+) plasma

36 ined as a B-cell neoplasm characterized by a lymphoplasmacytic infiltrate in bone marrow (BM) and IgM

37 which affected organs have a characteristic lymphoplasmacytic infiltrate rich in IgG4-positive cells

38 At the time of aortic surgery, a transmural lymphoplasmacytic infiltrate was detected in the patient

39 sease is characterized by a dense polyclonal lymphoplasmacytic infiltrate, and is frequently associat

40 vealed moderate cervical lymphadenopathy and lymphoplasmacytic infiltrate, but these were less extens

41 Human Abs cloned from MCB lymphoplasmacytic infiltrate-derived phage display libra

42 lobular hepatitis with acidophil bodies and lymphoplasmacytic infiltrate.

43 nority of breast cancers is characterized by lymphoplasmacytic infiltrates that have been correlated

44 losed moderate intraparenchymal fibrosis and lymphoplasmacytic infiltrates without lymphoid follicles

45 Diffuse lymphoplasmacytic infiltrates, presence of abundant IgG4

46 gM protein>/=3 g/dL and/or>/=10% bone marrow lymphoplasmacytic infiltration but no evidence of end-or

47 histopathological features of IgG4-RHP are a lymphoplasmacytic infiltration of IgG4-positive plasma c

48 WM is a B-cell neoplasm characterized by lymphoplasmacytic infiltration of the bone marrow and a

49 is characterized by a predominant polyclonal lymphoplasmacytic infiltration, and is frequently refrac

50 thology features of IgG4-related disease are lymphoplasmacytic infiltration, storiform fibrosis, and

51 Sclerosing lymphoplasmacytic inflammation at almost any site can re

52 patitic" pattern of injury, characterized by lymphoplasmacytic inflammation with necroinflammatory ac

53 Minimal to moderate lymphoplasmacytic inflammation, with a predilection for

54 ncommon and was seen in 42% of patients with lymphoplasmacytic lobular, portal, and interface hepatit

55 Lymphoplasmacytic lymphoma (LPL) is characterized by t(9

56 CD52 is expressed on malignant cells in lymphoplasmacytic lymphoma (LPL), including IgM-secretin

57 oglobulinemia is an incurable, IgM-secreting lymphoplasmacytic lymphoma (LPL).

58 mutation in 28.2% (37/131) of patients with lymphoplasmacytic lymphoma (Waldenstrom macroglobulinemi

59 igration of chronic lymphocytic leukemia and lymphoplasmacytic lymphoma cells, two other B cell malig

60 aldenstrom macroglobulinemia (WM) is a rare, lymphoplasmacytic lymphoma characterized by hypersecreti

61 strom macroglobulinemia (WM) is an incurable lymphoplasmacytic lymphoma with limited options of thera

62 phoma (28), marginal-zone lymphoma (15), and lymphoplasmacytic lymphoma with or without Waldenstrom's

63 d tissue marginal zone lymphoma, and 38 with lymphoplasmacytic lymphoma) who were randomly assigned t

64 acroglobulinemia (WM), a distinct subtype of lymphoplasmacytic lymphoma, early data on limited sequen

65 om macroglobulinemia (WM), an IgM-associated lymphoplasmacytic lymphoma, has witnessed several practi

66 specifically, chronic lymphocytic leukemia, lymphoplasmacytic lymphoma, marginal zone lymphoma, and

67 L), 13 had follicular lymphoma (FL), six had lymphoplasmacytic lymphoma, six had Hodgkin's disease (H

68 ent of Waldenstrom macroglobulinemia (WM), a lymphoplasmacytic lymphoma.

69 oglobulinemia (WM) is an incurable low-grade lymphoplasmacytic lymphoma.

70 ), multiple myeloma (MM; RR = 2.9; 1.9-4.3), lymphoplasmacytic lymphoma/Waldenstrom macroglobulinemia

71 r a better definition of the new category of lymphoplasmacytic lymphoma; the variants of mantle-cell

72 ion was 37 marginal zone lymphomas (MZLs), 2 lymphoplasmacytic lymphomas, 2 follicular lymphomas, 4 C

73 mucosa-associated lymphoid tissue lymphoma, lymphoplasmacytic lymphomas, and small lymphocytic leuke

74 considered an obligate precursor to several lymphoplasmacytic malignancies, including immunoglobulin

75 aracterized by cyclin D1 up-regulation and a lymphoplasmacytic morphology, but is also more frequentl

76 myeloma, where it is also associated with a lymphoplasmacytic morphology.

77 9 cats), lymphocytic hepatitis (in 6 cats), lymphoplasmacytic myocarditis (in 8 cats), and interstit

78 g follicular (n = 9), marginal zone (n = 4), lymphoplasmacytic (n = 1), or small lymphocytic lymphoma

79 ation) as having lymphoplasmacytoid (n =92), lymphoplasmacytic (n = 24), polymorphous (n = 9), or und

80 s type I [24 of 25 (96%)], with interstitial lymphoplasmacytic nephritis [23 of 25 (92%)], and glomer

81 by the dominant clones in the oligoclonal B lymphoplasmacytic response in both patients was not a ca

82 itis (AIP) has been divided into subtypes 1 (lymphoplasmacytic sclerosing pancreatitis) and 2 (idiopa

83 from patients with follicular, mantle cell, lymphoplasmacytic, small lymphocytic, or marginal zone l