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 We demonstrate a systemic lymphoplasmacytic and histiocytic arteritis and periarte

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

18 We genotyped lymphoplasmacytic cells from 175 WM patients and observe

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

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

21 d confers prosurvival signaling in malignant lymphoplasmacytic cells in Waldenstrom macroglobulinemia

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

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

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

25 he infiltration of the bone marrow by clonal lymphoplasmacytic cells that produce monoclonal immunogl

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

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

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

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

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

31 otubules and with clinical associations with lymphoplasmacytic disorders.

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

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

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

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

36 istortion of the crypts; (b) dense and basal lymphoplasmacytic infiltrate and (c) scarcity of eosinop

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

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

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

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

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

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

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

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

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

46 lobular hepatitis with acidophil bodies and lymphoplasmacytic infiltrate.

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

48 losed moderate intraparenchymal fibrosis and lymphoplasmacytic infiltrates without lymphoid follicles

49 Diffuse lymphoplasmacytic infiltrates, presence of abundant IgG4

50 he multivariate analysis demonstrated tissue lymphoplasmacytic infiltration (OR 88.38, 95% CI 7.98-97

51 obulin M 4,500 mg/dL or greater, bone marrow lymphoplasmacytic infiltration 70% or greater, beta2-mic

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

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

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

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

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

57 c presentation was rectal ulcer (61%). Basal lymphoplasmacytic inflammation and mild crypt distortion

58 Sclerosing lymphoplasmacytic inflammation at almost any site can re

59 AIH-like lymphoplasmacytic inflammation with mild fibrosis was th

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

61 Minimal to moderate lymphoplasmacytic inflammation, with a predilection for

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

63 Lymphoplasmacytic lymphoma (LPL) is an incurable low-gra

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

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

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

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

68 144 months after diagnosis, in 1 patient to lymphoplasmacytic lymphoma and in 2 patients to multiple

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

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

71 transformation and leveraged these to model lymphoplasmacytic lymphoma in mice, based on mutated MYD

72 ld Caucasian male with a history of relapsed lymphoplasmacytic lymphoma was admitted to the hospital

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

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

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

76 age in elderly individuals and patients with lymphoplasmacytic lymphoma, a singular disease for study

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

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

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

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

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

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

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

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

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

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

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

88 sentative microscopic lesions were gastritis lymphoplasmacytic, moderate, multifocal, with perivascul

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

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

91 9 cats), lymphocytic hepatitis (in 6 cats), lymphoplasmacytic myocarditis (in 8 cats), and interstit

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

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

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

95 ificant differences were observed in overall lymphoplasmacytic or mast cell densities, nor in B cell

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

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

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