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1.
Int J Lab Hematol ; 39(3): 337-346, 2017 Jun.
Article in English | MEDLINE | ID: mdl-28263031

ABSTRACT

INTRODUCTION: The enumeration and differentiation of nuclear elements in synovial fluid is a cornerstone for diagnosis and follow-up of many orthopedic and rheumatologic diseases. In this study, we evaluated the analytical performance of Mindray BC-6800 BF mode (BC-6800-BF) for synovial fluid analysis. METHODS: Overall, 78 synovial fluids were collected and analyzed with both BC-6800-BF and light microscopy. The study also entailed the assessment of limit of blank (LoB), limit of detection (LoD), limit of quantification (LoQ), carryover and linearity. RESULTS: The LoB for the parameters total cells and white blood cells was 6 × 106 cells/L, and the LoD and LoQ were instead 15 and 16 × 106 cells/L, respectively. Linearity was excellent and carryover was negligible. The agreement between BC-6800-BF and light microscopy was satisfactory for all samples pretreated with hyaluronidase, displaying a bias between -5.9% and 8.2%. CONCLUSIONS: The use of BC-6800-BF for synovial fluid analysis enables rapid and accurate assessment, especially for total cell and polymorphonuclear counts. The use of BC-6800-BF may therefore allow the replacement of optical analysis, especially in samples pretreated with hyaluronidase, thus allowing its routine use for the screening of synovial specimens.


Subject(s)
Flow Cytometry/instrumentation , Flow Cytometry/methods , Rheumatic Diseases/metabolism , Synovial Fluid/metabolism , Female , Humans , Hyaluronoglucosaminidase/chemistry , Leukocytes/metabolism , Leukocytes/pathology , Male , Middle Aged , Rheumatic Diseases/pathology
2.
Int J Lab Hematol ; 38(1): 90-101, 2016 Feb.
Article in English | MEDLINE | ID: mdl-26547138

ABSTRACT

INTRODUCTION: An accurate and rapid analysis of cells in body fluids (BFs) is important for diagnosis and follow-up in many pathological conditions. We evaluated the analytical performance of the module BF Mindray BC-6800 (BC-6800-BF) for cytometric analysis of ascitic and pleural fluids. METHODS: A total of 99 ascitic and 45 pleural samples were collected and assessed with BC-6800-BF and optical microscopy. This study also includes the evaluation of limit blank (LoB), limit detection (LoD), limit quantitation, (LoQ), carryover, linearity, and diagnostic concordance between the two methods. RESULTS: For TC-BF, LoB was 1 × 10(6) cells/L, LoD was 3 × 10(6) cells/L, and LoQ was 4 × 10(6) cells/L. Linearity was excellent (r(2) = 0.99) and carryover was negligible. TC-BF performed with the two methods showed Pearson's correlation of 0.99 (P < 0.0001), Passing-Bablok regression y = 1.04x - 1.17, and bias 33.7 cells. In ascitic fluids, polymorphonuclear cells (PMN) showed an area under curve (AUC) of 0.98 (P < 0.0001). In pleural fluids, mononuclear cells (MN) and PMN % displayed an AUC of 0.79 (P < 0.0001) and 0.93 (P < 0.0001), respectively. CONCLUSIONS: BC-6800-BF in ascitic and pleural fluids offers rapid and accurate cell and differential counts in clinically relevant concentration ranges. The use of BC-6800-BF may allow to replace routine optical counting, except for samples displaying abnormal cell counts or abnormal DIFF scattergram.


Subject(s)
Body Fluids/cytology , Cell Count/methods , Cell Count/standards , Pleural Effusion/diagnosis , Ascitic Fluid/cytology , Ascitic Fluid/pathology , Automation, Laboratory , Biomarkers , Cell Count/instrumentation , Humans , Pleural Effusion/pathology , Reproducibility of Results , Sensitivity and Specificity
3.
Ann Oncol ; 19(11): 1842-6, 2008 Nov.
Article in English | MEDLINE | ID: mdl-18550574

ABSTRACT

BACKGROUND: Sentinel lymph node biopsy (SLNB) was developed to axillary lymph node dissection (ALND) in the treatment of breast cancer. SLNB is predictive of axillary node status. Major concern is the occurrence of a false-negative SLN. Purpose of this study is to determine the rate of axillary recurrence in our series of unselected patients. PATIENTS AND METHODS: All patients with a negative SLNB from November 1999 to December 2006 have been treated and followed at our unit. Information on patients' characteristics, treatment and follow-up has been collected. RESULTS: Eight-hundred and four patients with negative SLNB did not receive ALND. After a median follow-up of 38.8 months, 21 patients had distant metastases, four had axillary relapse, nine had an in-breast recurrence and two had both. All patients with axillary recurrence received axillary dissection and systemic adjuvant therapy. They are all presently alive and free from disease. CONCLUSION: Data from this series, the largest from a general hospital, showed that isolated axillary node recurrence after negative SLNB is rare (<1%) and comparable with those reported from referral cancer institutions. We confirm that SLNB for the treatment of early breast cancer patients of a community-based hospital is safe and reliable.


Subject(s)
Breast Neoplasms/pathology , Lymph Nodes/pathology , Neoplasm Recurrence, Local/pathology , Adult , Aged , Axilla , Breast Neoplasms/radiotherapy , Breast Neoplasms/surgery , Disease-Free Survival , Female , Humans , Lymphatic Metastasis , Middle Aged , Radiotherapy, Adjuvant , Sentinel Lymph Node Biopsy
4.
Acta Otorhinolaryngol Ital ; 24(4): 223-5, 2004 Aug.
Article in English | MEDLINE | ID: mdl-15688908

ABSTRACT

Follicular dendritic cell tumour/sarcoma is a rare tumour involving lymph-node or extra-lymph-node sites; review of the literature reveals very few cases of follicular dendritic cell tumour, probably since, in the past, the disease has often been mistaken for other neoplasms: low differentiated carcinomas and fusate cell carcinomas, sarcomas, melanomas, thymic neoplasms, Castle carcinoma and other dendritic cell tumours (especially interdigital cell tumour/sarcoma). In the case described here, attention is focused on the diagnostic difficulties and on the therapeutic profile, comparing data with those reported in the international literature.


Subject(s)
Dendritic Cells, Follicular/pathology , Lymph Nodes/pathology , Adenoma/pathology , Biopsy, Needle , Female , Humans , Lymph Nodes/surgery , Middle Aged , Neck , Thyroid Neoplasms/pathology
5.
Dermatology ; 200(2): 115-9, 2000.
Article in English | MEDLINE | ID: mdl-10773698

ABSTRACT

BACKGROUND: Asymptomatic blisters on psoriatic plaques are an uncommon adverse effect of TL-01 (UVB narrow-band 312 nm) phototherapy. OBJECTIVE: We report 7 new cases aiming to clarify the pathogenesis. METHODS: Blisters were biopsied at different times after onset. Blood porphyrins and antibodies to nuclear antigens and the cell surface of keratinocytes were investigated. RESULTS: We observed 7 asymptomatic blistering eruptions strictly limited to recovering psoriatic plaques. Biopsies taken within 24 h showed junctional detachment and apoptotic necrosis of basal keratinocytes. After 48 and 72 h, the blisters were intraepithelial, due to basal cell regeneration, and were no longer evident at 96 and 120 h. Dermal inflammation was always mild. Direct immunofluorescence tests as well as stainings for p53 protein did not show substantial changes. Blood investigations were negative. CONCLUSIONS: TL-01 blisters are caused by the quick reduction of acanthosis and desquamation before defensive mechanisms, i.e. the increase in the thickness of the stratum corneum and pigmentation, develop. However, the pathogenetic mechanisms of apoptosis of keratinocytes remain unknown.


Subject(s)
Blister/etiology , Psoriasis/radiotherapy , Ultraviolet Therapy/adverse effects , Adolescent , Adult , Aged , Apoptosis , Autoantibodies/analysis , Blister/pathology , Female , Humans , Immunohistochemistry , Keratinocytes/immunology , Keratinocytes/pathology , Ki-67 Antigen/analysis , Male , Middle Aged , Porphyrins/blood , Prospective Studies , Psoriasis/blood , Psoriasis/immunology , Psoriasis/pathology , Skin/pathology
6.
Am J Dermatopathol ; 22(1): 1-6, 2000 Feb.
Article in English | MEDLINE | ID: mdl-10698208

ABSTRACT

We evaluated the incidence, morphology, and immunophenotype of intraepidermal collections of mononuclear cells (ICMC) in a large number of inflammatory dermatosis and cutaneous lymphomas. ICMC appeared as small to large aggregates of cells, showing a morphology variable from monocytes to obvious dendritic cells, admixed with rare lymphocytes. ICMC were recognized in the epidermis or within hair follicle epithelium, and were either loosely or compactly arranged. ICMC were identified in 124 of 1,248 skin biopsies (9.9%) of inflammatory or lymphoid infiltrates, and were particularly frequent in spongiotic (43.4%) and in lichenoid dermatitis (10%), whereas they were rarely found in nonspecific superficial dermatitis (3.8%) and in psoriasis (4.7%). ICMC were also frequent in cutaneous T-cell lymphoma (13.3%), where they mimicked Pautrier abscesses. The ICMC forming cells showed a unique phenotype: the majority of them expressed CD1a and S-100, and lacked CD14, similar to mature Langerhans cells, but they were also strongly labeled by anti-CD11b, anti-CD36, and anti-CD68. Moreover, a subpopulation of them expressed CD83, an antigen that is usually absent on Langerhans cells. The occurrence of ICMC is a rather frequent, although hitherto poorly studied, phenomenon, occurring in several dermatosis, but particularly frequent in spongiosis-associated skin reactions. The cells within ICMC are represented by dendritic cells and dendritic cell precursors, whose phenotype indicates their derivation from circulating monocytes and differentiation into mature Langerhans cells.


Subject(s)
Epidermis/pathology , Langerhans Cells/pathology , Monocytes/pathology , Skin Diseases/pathology , Antigens, CD/analysis , Dendritic Cells/pathology , Humans , Immunohistochemistry , Immunophenotyping , Monocytes/immunology , Mycosis Fungoides/pathology , Skin Diseases/immunology , Skin Neoplasms/pathology
8.
Arch Ital Urol Androl ; 69(2): 101-4, 1997 Apr.
Article in Italian | MEDLINE | ID: mdl-9213493

ABSTRACT

Recent application of molecular cytogenetic techniques to the evaluation of epithelial renal cell tumors have showed some characteristic combinations of genetic alterations within the chromosomal DNA. Moreover each group of abnormalities has been correlated with peculiar tumor morphology. The new classification of renal cell neoplasms proposed by G. Kovacs, based on specific genetic alterations, and histologic pattern, together with the morphologic and pathologic features that correlate with survival has been discussed.


Subject(s)
Carcinoma, Renal Cell/pathology , Kidney Neoplasms/pathology , Neoplasms, Glandular and Epithelial/pathology , Carcinoma, Renal Cell/classification , Chromosomes/chemistry , Chromosomes/ultrastructure , DNA, Neoplasm/chemistry , Humans , Kidney Neoplasms/classification , Neoplasms, Glandular and Epithelial/classification , Prognosis
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