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Jacqueline Zanen

Publications and source records attributed to Jacqueline Zanen.

2 recordsLinked to original sources

Pulmonary emphysema: objective quantification at multi-detector row CT--comparison with macroscopic and microscopic morphometry.

PURPOSE: To prospectively compare pulmonary function tests and helical computed tomographic (CT) indexes for quantifying pulmonary emphysema with macroscopic and microscopic morphometry. MATERIALS AND METHODS: The investigation was approved by the local ethics committee, and written informed consent was obtained from patients. Multi-detector row CT of the thorax was performed with simultaneous acquisition of four 1-mm sections in 80 patients (57 men, 23 women; age range, 38-79 years) referred for surgical resection of lung cancer. From the raw data, 1.25-mm-thick sections were reconstructed at 10-mm intervals. Relative areas of lung with attenuation coefficients lower than nine thresholds and eight percentiles of the distribution of attenuation coefficients were calculated. Relative areas and percentiles were compared with areas found macroscopically to have emphysema and with two microscopic indexes assessed on resected specimens. Pulmonary function tests were measured 24-48 hours before surgery. Spearman correlation coefficients were calculated between each set of CT data obtained with the nine tested thresholds and eight percentiles with macroscopic and microscopic measurements. RESULTS: For relative lung areas, the strongest correlation with macroscopy was observed with a threshold of -970 HU (r = 0.543, P < .001) and that with microscopy was observed at -960 and -970 HU, depending on the index considered (r = 0.592, P < .001 and r = -0.546, P < .001, respectively). For percentiles, 1st percentile showed the strongest correlation with both macroscopy (r = -0.463, P < .001) and microscopy (r = -0.573, P < .001; and r = 0.523, P < .001 for each microscopic measurement). Forced expiratory volume in 1 second and vital capacity ratio, diffusing capacity of lung for carbon monoxide, and each of the three CT indexes were complementary to predict microscopic indexes. CONCLUSION: Relative lung areas with attenuation coefficients lower than -960 or -970 HU and 1st percentile are valid indexes to quantify pulmonary emphysema on multi-detector row CT scans.

Adult↗

Phenotypic variations and dynamic topography of transformed cells in an experimental model of diethylstilbestrol-induced renal tumour in male Syrian hamster.

This work explores the phenotypic changes affecting transformed cells in an experimental model of diethylstilbestrol (DES)-induced renal tumours in male Syrian hamster. This estrogen-induced neoplasm presents an important cytological pleomorphism and its origin remains largely controversial. In order to characterize phenotypic variations during tumour progression, the occurrence of seven lineage markers was analysed by a morphometric approach in kidney sections of DES-exposed hamsters (6-11 months). S100 protein, neuron-specific enolase (NSE) and vimentin are expressed by a large percentage of malignant cells during tumour development. Glial fibrillary acidic protein (GFAP), protein gene product 9.5 (PGP 9.5) and desmin are mostly evidenced in advanced neoplasm whereas Leu 7 always presents a focal expression. As evidenced by double-label immunofluorescence, the coexpression of three important neuroectodermal lineage markers (S100, NSE and PGP 9.5) in earliest tumour buds points to a peripheral nerve sheath origin for this neoplasm thus confirming previously published data. For each marker, the fluctuations of expression levels during tumour progression as well as the spatial heterogeneity of distribution suggest variable phenotypic differentiation of transformed cell populations. This observation is largely corroborated by double-label immunofluorescence showing coexpression modification of several markers during tumour progression. This points to a complex dynamic and spatial self-organization of different phenotypes within neoplasms. Altogether, these results support the concept that DES-induced kidney tumours are not made of unstructured cell populations but represent adaptive complex dynamic biosystems.

Animals↗