CD 138, syndecan I
The syndecans are a family of four transmembrane glycoproteins. Syndecans 1 and 2 appear to be altenatively expressed: syndecan 1 is the major syndecan in epithelial cells while syndecan 2 is more abundantly expressed in mesothelium and mesenchymal cells10.
Syndecan 1, CD138, is a 220 kd sulphate-rich proteoglycan adhesion molecule expressed in the late stages of B-cell differentiation, acquired as they differentiate towards plasma cells. Syndecan is up-regulated by WT-1 and in turn acts as a receptor for collagen, fibronectin and thrombospondin3. It binds basic fibroblast growth factor, an angiogenic agent, and thereby modulates neovascularisation6. The free ectodomain of syndecan I suppresses proliferation of tumour cells6.
Immunohistochemical expression
Antigen retrieval is required for formalin-fixed tissue and enhances staining of B-5 fixed tissue4.
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non-neoplastic plasma cells4
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squamous epithelium of tonsils, skin and adnexa, prostatic glands and Hassall corpuscles4.
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Leydig cells1
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Neuronal cells1
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Endothelial and stromal cells during wound healing1
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other components of bone marrow and lymph nodes - lymphocytes, dendritic and reticulum cells, endothelial cell, myeloid cells, erythroblasts and megakaryocytes are NEGATIVE1.
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myeloma1,4 Reactivity appears to be rapidly lost in unfixed cells subject to flow cytometry1.
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Reed-Sternberg cells1
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immunoblastic lymphoma with plasmacytoid differentiation: 5/13 cases1
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Haematolymphoid disorders
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CD138
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Multiple myeloma
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8/81,
43/43(in bone marrow biopsy: strong positivity with membrane accentuation in all cases)4,
2/16(both positive cases had plasmacytoid morphological features)4,
1/1(strong positivity)9
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Plasmacytoid lymphoma
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2/21,
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Lymphoplasmacytic lymphoma
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9/9(positivity restricted to mature plasma cells)1,
4/4(reactivity restricted to plasma cell component)4,
3/3(strong positivity)9
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Acute lymphoblastic leukaemia
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0/3(in bone marrow biopsy)4
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Acute myelogenous leukaemia
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0/13(in bone marrow biopsy)4
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Chronic myelogenous leukaemia
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0/2(in bone marrow biopsy)4
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CLL/small lymphocytic lymphoma
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0/201,
0/5(in bone marrow biopsy)4, 0/144,
11/11(B-CLL, strong positivity after antigen retrieval at high temperature in a pressure cooker using citrate solution)9
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Follicular lymphoma
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0/181,
0/2(in bone marrow biopsy)4, 0/44,
0/14(on tissue microarray)4, 0/79
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Marginal zone lymphoma
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0/31,
4/6(3/3 extranodal and 1/1 nodal showed strong positivity for the extensive clonal plasmacytic component. 2 splenic cases were negative)4, 0/69
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Mantle cell lymphoma
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0/121,
0/1(in bone marrow biopsy)4, 0/44, 0/99
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Hairy cell leukaemia
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0/2(in bone marrow biopsy)4
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DLBCL
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5/35(positivity restricted to immunoblastic lymphomas with plasmacytoid features)1,
0/1(in bone marrow biopsy)4,
2/16(positivity restricted to the only two cases with plasmacytoid features)4,
1/44(on tissue microarray positivity restricted to the one case with plasmacytoid features)4, 1/147, 0/22, 0/59
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Mediastinal large B-cell lymphoma
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0/14, 0/19
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Burkitt's lymphoma
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0/71,
0/1(in bone marrow biopsy)4, 0/12, 0/39
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B-cell Lymphoma NOS
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0/39
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Precursor T-lymphoblastic lymphoma
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0/29
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Peripheral T-cell lymphoma
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0/151,
0/1(in bone marrow biopsy)4, 0/14, 0/19
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Mycosis fungoides
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0/44
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Angioimmunoblastic lymphoma
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0/19
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T-cell Lymphoma NOS
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0/19
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Anaplastic large cell lymphoma
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0/51, 0/34, 0/39
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Mycosis fungoides
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0/71
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Post transplant lymphoproliferative disease
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0/24
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Nodular lymphocyte predominant Hodgkin disease
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0/61, 0/34,
0/2(on tissue microarray)4
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Classical Hodgkin disease
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23/311,
0/16(in 11 cases, the fibroblasts and collagen bands stained)4
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Mast cell disease
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0/1(in bone marrow biopsy)4
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Langerhans cell histiocytosis
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0/14
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Non-neoplastic disease
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0/3(in bone marrow biopsy: erythroid hyperplasia, myeloid hyperplasia and a remission marrow following AML)4,
0/14(5 reactive lymphadenopathy, 2 HIV-related lymphadenopathy, 1 CMV lymphadenitis, 1 dermatopathic lymphadenitis, 1 granulomatous lymphadenitis, 1 infectious mononucleosis, 1 Rosai-Dorfmann disease [ delicate stromal positivity], 1 Castleman disease [delicate stromal positivity] and 1 Kikuchi's disease)4
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Non-haematolymphoid disorders
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CD138
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Reactive mesothelial proliferation
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0/11(5 pleural, 2 peritoneal, 1 pericardial effusions and 3 peritoneal washings)2
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Malignant mesothelioma
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2/24(in two cases, staining was moderate or strong but of <5% of cells)2, 1/213,
2/2(focal weak staining)4,
52/57(using frozen sections: sarcomatoid mesotheliomas showed weaker staining than did epithelial or biphasic cases)6
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Metastatic carcinoma, overall
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32/58(most cases showed strong staining, of a variable percentage of cells)2
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Lung
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adenocarcinoma
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8/122, 11/213
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squamous cell carcinoma
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4/42, 1/12
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non-small cell carcinoma. NOS
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5/5(4 primary, 1 metastatic: membranous and granular cytoplasmic staining in one case: all also showed stromal staining)4
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small cell carcinoma
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2/22, 1/12, 0/63,
1/2(metastases: positivity in viable and necrotic cells: 2 cases also showed stromal staining)4
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sarcomatoid carcinoma
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1/12
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poorly differentiated with neuroendocrine features
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0/12
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carcinomas overall
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11/162, 11/273
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pleuropulmonary blastoma
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0/12
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Ovary
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papillary serous
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8/152
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endometrioid
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1/12
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clear cell
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1/12
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mixed Mullerian tumour
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012
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poorly differentiated carcinoma
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1/12
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overall
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8/112, 10/243
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Skin
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squamous cell carcinoma
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25/253
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basal cell carcinoma
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14/203
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Merkel cell carcinoma
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2/93
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Thyroid
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follicular adenoma
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10/243
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papillary carcinoma
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2/93, 1/14
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medullary carcinoma
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2/173, 2/24
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Salivary gland tumour
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various
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3/113
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myoepithelioma
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1/1with marked plasmacytoid morphology: diffuse strong membranous positivity)4
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Larynx
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squamous cell carcinoma
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3/32,
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Breast
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ductal and lobular carcinomas
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4/42, 2/62, 18/263,
4/6(in bone marrow biopsy: in some cases, the morphology of the tumour cells could be confused with plasma cells)4,
8/9(7 cases also showed stromal staining)4
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Pancreas
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adenocarcinoma
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1/32, 4/133
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Colon
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adenocarcinoma
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5/51, 0/32, 9/103,
3/3(1 case also showed stromal staining)4
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Uterus
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endometrioid adenocarcinoma
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2/32, 9/103
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Oesophagus
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adenocarcinoma
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2/22,
0/1(in bone marrow biopsy)4
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Kidney
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renal cell carcinoma
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12/193,
1/1(metastatic: focal weak staining)4
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Bladder
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transitional cell carcinoma
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1/22, 22/243, 3/34
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Prostate
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adenocarcinoma
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1/22, 6/183,
1/1(in bone marrow biopsy)4
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Stomach
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adenocarcinoma
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0/12, 2/153,
4/5(metastases: positivity in viable and necrotic cells: one case also showed stromal staining)4
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Liver
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hepatocellular carcinoma
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15/253, 2/24
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cholangiocarcinoma
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1/12, 13/143
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embryonal sarcoma
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0/12
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Adrenal
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cortical tumour
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7/203
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Phaeochromocytoma
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0/24
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Thymoma
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0/83,
1/1(showed both tumour cell and stromal staining)4
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Germ cell tumour, NOS
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0/143
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Seminoma
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0/14
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Schwannoma
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0/14
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GIST
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1/1(weak focal staining)4
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Leiomyosarcoma
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1/2(metastatic)4
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Abdominal angiosarcoma
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0/12
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Synovial sarcoma
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2/2(a biphasic case showed strong membranous staining in the epithelial component and membranous and cytoplasmic staining of the spindle cell component. A monophasic case showed membranous and cytoplasmic staining)4
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Epithelioid sarcoma
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0/103
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Neuroendocrine carcinoma
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3/93,
0/1(in bone marrow biopsy)4
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Carcinoid tumour
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3/32, 2/103
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Malignant melanoma
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1/12,
0/1(metastatic melanoma)2, 1/203,
5/10(moderate to strong membranous staining)4
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Notes:
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any degree of membrane staining was considered positive2
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Loss of CD138 immunoreactivity in carcinomas may be associated with dedifferentiation9 or tumour progression.
Adenocarcinomas and mesotheliomas may show differences in the relative expression of syndecans 1 and 210:
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Reference 10
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Adenocarcinoma
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Mesothelioma
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Syndecan 1 > syndecan 2
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8
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0
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Syndecan 1 = syndecan 2
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0
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0
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Syndecan 1 < syndecan 2
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2(both these adenocarcinomas were poorly differentiated)
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8
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Diagnostic utility
Note that a number of non-haematolymphoid neoplasms (myoepithelioma, medullary carcinoma of thyroid, melanoma) may have a plasmacytoid morphology and may also be positive for CD138: an appropriate panel of antibodies needs to be sued.
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Identifying and quantifying plasma cells in bone marrow samples1.
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In mature B-cell neoplasms, immunoreactivity indicates plasma cell and/or postfollicular differentiation.
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Possibly in the differentiation of adenocarcinoma (positive in 55% of cases) from mesothelioma (usually negative) but the data currently available is inadequate.
References
1 Costes V, Magen V, Legouffe E et al. The Mi15 monoclonal antibody (anti-syndecan-1) is a reliable marker for quantifying plasma cells in paraffin-embedded bone marrow biopsy specimens. Human Pathology 1999;30:1405-11. xxxxxxxxxx
2 Saqi A, Yun SS, Yu GH, et al. Utility of CD138 (syndecan-1) in distinguishing carcinomas from mesotheliomas. Diagn Cytopathol 2005; 33:65-70
3 Chu PG, Arber DA,Weiss LM. Expression of T/NK-cell and plasma cell antigens in nonhematopoietic epithelioid neoplasms. An immunohistochemical study of 447 cases. Am J Clin Pathol 2003; 120:64-70
4 O'Connell FP, Pinkus JL,Pinkus GS. CD138 (syndecan-1), a plasma cell marker immunohistochemical profile in hematopoietic and nonhematopoietic neoplasms. Am J Clin Pathol 2004; 121:254-63
5 Shah L, Walter KL, Borczuk AC, et al. Expression of syndecan-1 and expression of epidermal growth factor receptor are associated with survival in patients with nonsmall cell lung carcinoma. Cancer 2004; 101:1632-8
6 Kumar-Singh S, Jacobs W, Dhaene K, et al. Syndecan-1 expression in malignant mesothelioma: correlation with cell differentiation, WT1 expression, and clinical outcome. J Pathol 1998; 186:300-5
7 Chilosi M, Adami F, Lestani M, et al. CD138/syndecan-1: a useful immunohistochemical marker of normal and neoplastic plasma cells on routine trephine bone marrow biopsies. Mod Pathol 1999; 12:1101-6 xxxxxxxxxx
8 Sebestyen A, Kovalszky I, Mihalik R, et al. Expression of syndecan-1 in human B cell chronic lymphocytic leukaemia. Eur J Cancer 1997; 33:2273-7 xxxxxxxxxx
9 Sebestyen A, Berczi L, Mihalik R, et al. Syndecan-1 (CD138) expression in human non-Hodgkin lymphomas. Br J Haematol 1999; 104:412-9
10 Gulyas M,Hjerpe A Proteoglycans and WT1 as markers for distinguishing adenocarcinoma, epithelioid mesothelioma, and benign mesothelium. J Pathol 2003; 199:479-87
This page last revised 1.11.2005.
©SMUHT/PW Bishop