Biomedical subjects

P Rippstein

Publications and source records attributed to P Rippstein.

23 records · Page 2Linked to original sources

PubMedDate not supplied

A quantitative comparison of light and electron microscopic diagnoses in specimens obtained by fine-needle aspiration biopsy.

Because fine-needle aspiration biopsy (FNAB) is being increasingly used as a primary diagnostic tool, it is essential to obtain the maximum information from the aspirate. Electron microscopy is an adjunctive procedure that is readily applied to FNAB specimens. The value of electron microscopy to the cytopathologist was assessed by comparing the initial, tentative, or interim diagnosis based on light microscopic features with the diagnosis resulting from the ultrastructural characteristics of needle rinse material. Over a 3-year period, 279 FNAB specimens obtained under radiologic control were examined ultrastructurally; of these, 57 (20.4%) were considered inadequate specimens for diagnostic purposes. The remaining 222 FNAB specimens were segregated into four groups: 17 cases (7.7%) in which electron microscopy played a major role because the final diagnosis was unsuspected from light microscopy; 43 cases (19.4%) in which electron microscopy selected a specific diagnosis from a set of differential diagnoses or provided additional information that was clinically relevant; 45 cases (20.3%) in which additional diagnostic information was obtained by electron microscopy but was not clinically relevant; and 117 cases (52.6%) in which electron microscopy was not helpful because the light and electron microscopic diagnoses were the same. In this comparative study, electron microscopy provided a major contribution to the final cytologic diagnosis in 27.1% of the cases (groups 1 and 2). Descriptive examples illustrate how the architectural and cytologic features revealed by electron microscopy assist in establishing the final diagnosis. Examination of needle rinse specimens, particularly aspirates from lung and liver, indicates that most FNABs provide mini-surgical biopsy specimens that are well suited to ultrastructural examination.

Adult↗

PubMedDate not supplied

Immunogold localization of actin and cytokeratin filaments in myoepithelium of human parotid salivary gland.

Myoepithelial cells of salivary gland are uniquely specialized cells; their function is unclear, but the considerable complement of muscle-specific actin suggests contractility is one function. By routine transmission electron microscopy myofilament visualization is variable. Some myoepithelial cells appear to have limited and only focal aggregates of myofilaments, while others seem to have readily appreciated myofilaments within a longitudinally oriented cytoplasmic zone at the basal portion of the cell. However, immunogold electron microscopy using the anti-muscle-specific actin antibody, HHF35, while indicating a basal distribution for the muscle-isoform of actin in a platelike fashion in certain myoepithelial cells, also reveals that others associated with both intercalated ducts and acini have a more generalized distribution of myofilaments throughout the cytoplasm. Actin was also noted within tonofilaments and double immunogold labeling using both the HHF35 and AE1/AE3 (anticytokeratins) antibodies confirmed the variable interrelationship of these two filaments. Within any one myoepithelial cell, actin and cytokeratins might colocalize in some areas of the cytoplasm containing filaments, but not in adjacent zones. These results suggest that intermediate filaments and myofilaments are complexly organized in myoepithelial cells, and that quantitative and qualitative differences exist in the expression and distribution of intermediate filaments and myofilaments. These cells are likely structurally, if not functionally, heterogeneous.

Actins↗

PubMedDate not supplied

Reliability of criteria for ultrastructural identification of neuroendocrine granules.

For full diagnostic use to be made of the neurosecretory granule, the range of sizes, forms, and staining qualities for this cytoplasmic organelle, along with the extent of its expression in various neoplasms, must be established. Neurosecretory type granules occasionally occur in nonneuroendocrine tumors. A series of carcinoids of the lung provides a model for assessing the morphologic types of cytoplasmic granules identified by antibodies to chromogranin A and immunogold labeling. The results show that granule structure in tumors is pleomorphic. Despite having sizes within the expected range, many labeled and, indeed, unlabeled secretory granules are atypical, particularly in structural form. Cell-to-cell variation in the proportion of even typical neurosecretory granules labeling for chromogranin A is the rule. Studies correlating biochemical, immunohistochemical, electron microscopic, and perhaps in situ hybridization characteristics are required to define better the criteria for unequivocal identification of neurosecretory granules in tumors.

Adenocarcinoma↗

PubMedDate not supplied

Intracisternal collagen fibrils in proliferative fasciitis and myositis of childhood.

During ultrastructural examination of a difficult to diagnose tumor, short spacing collagen fibrils (periodicity of banding, approximately 43.2 nm) and native collagen fibrils (periodicity of banding, approximately 53 nm) were found in dilated and vacuolated cisternae of rough endoplasmic reticulum and the perinuclear cistern. Original diagnoses from several histopathologists included alveolar soft part sarcoma, malignant fibrous histiocytoma, atypical fibroxanthoma, and myogenic tumor. The finding of intracisternal collagen (which is but a variety of intracellular collagen) led to the conclusion that this was a fibroblastic neoplasm. This, plus a review of the histologic findings, led to the diagnosis of proliferative fasciitis and myositis of childhood.

Adolescent↗

PubMedDate not supplied

Evaluation of apoptosis in four human tumour cell lines with differing sensitivities to cisplatin.

Four human tumour cell lines were evaluated for their ability to undergo apoptosis when subjected to cisplatin or hyperthermia treatment. In an ovarian carcinoma line (A2780s) and its derivative cisplatin resistant line (A2780cp) the variation in response was expressed for both the colony survival endpoint and the apoptosis endpoint. Apoptosis was measured by the number of floating cells, DNA agarose gels, and electron microscopy. In fact, cisplatin resistance was expressed to a higher level for apoptosis, than colony survival in the A2780cp cell line compared to the A2780s line. The melanoma cell line (Sk Mel-3) also showed induced apoptosis by cisplatin treatment while the glioma line (U87MG) showed little to no apoptosis in response to cisplatin treatment. Hyperthermia (43 degrees C for 1 hour) induced apoptosis in the human melanoma cell line but not in the glioma cell line. These data indicate that, while both cisplatin and hyperthermia can induce apoptosis in human tumour cell lines, the degree of induction is highly cell line dependent.

Antineoplastic Agents↗