scholarly journals Honeycomb appearance of fetal myofibromatosis

2019 ◽  
Vol 53 (4) ◽  
pp. 549-551 ◽  
Author(s):  
M. Pekar‐Zlotin ◽  
O. Levinsohn‐Tavor ◽  
A. Livneh ◽  
O. Sher ◽  
Y. Melcer ◽  
...  
Keyword(s):  
2012 ◽  
Vol 10 (3) ◽  
pp. A25 ◽  
Author(s):  
Yuko Tokuhisa ◽  
Masaki Shimizu ◽  
Akihiro Yachie

Nature ◽  
1890 ◽  
Vol 43 (1098) ◽  
pp. 30-30
Author(s):  
J. SHAW
Keyword(s):  

2006 ◽  
Vol 26 (2) ◽  
pp. 158-160 ◽  
Author(s):  
Toshihiko Kubota ◽  
Asao Hirano ◽  
Ryuichi Tanaka ◽  
Hitoshi Takahashi

1966 ◽  
Vol 28 (3) ◽  
pp. 449-460 ◽  
Author(s):  
Hideyuki Tsukada ◽  
Yohichi Mochizuki ◽  
Seiki Fujiwara

The nucleoids of microbodies of rat liver cells were isolated in a highly homogeneous and pure state, by treating the microbody-rich fraction, prepared from 10% polyvinylpyrrolidone-0.25 M sucrose homogenate, with Triton X-100. Three treatments with 0.1% detergent were enough to render the nucleoids free from contamination with mitochondria, microsomes, lysosomes, and intact microbodies. Electron microscopically, the nucleoids were found to consist of parallel bundles of highly dense hollow tubules, the outer and inner diameters of which are approximately 150 and 50 A, respectively. Ten tubules are arranged around a longitudinal space 190 x 200 A in width. The nucleoids thus show a honeycomb appearance in the cross-plane and a parallel-packed structure in the longitudinal plane. Biochemically, the nucleoids were found to bear only urate oxidase among probably microbody-enzymes, and they might be the only cytoplasmic particles of rat liver cells in which the enzyme locates. Urate oxidase activity, on a unit protein basis, of the nucleoid preparation is approximately 380 times as high as that of the whole homogenate, and is almost comparable with that of a commercial type I enzyme preparation. No enzymes of mitochondrial, microsomal, and lysosomal origins were detected in the nucleoids. The fine structure of the nucleoids is described in detail, and a probable schematic diagram is presented.


2013 ◽  
Vol 163 (3) ◽  
pp. S110
Author(s):  
N. Bayar ◽  
İ.Ö. Yüksel ◽  
A. Yılmaz ◽  
S. Arslan

2019 ◽  
Vol 22 (2) ◽  
pp. 186-192 ◽  
Author(s):  
Mathieu Harel ◽  
Chloe Touzet ◽  
Anthony Barthélemy ◽  
Emilie M Ségard-Weisse

Objectives The aim of this study was to report the prevalence of a honeycomb appearance of the spleen in a population of referral cats presented for ultrasound examination, and to determine the diagnostic value of this finding vs the definitive diagnosis, the splenic cytological and haematological results. Methods Data were obtained from the medical records (2016–2018) of cats that had an ultrasonographic honeycomb appearance of the spleen, a splenic cytological diagnosis and a complete blood count. Results Twenty-five cats were included. Prevalence of the honeycomb pattern was 6.8%. None of the spleen was considered normal on cytology and four types of lesions were found: lymphoid hyperplasia (64%), neoplasia (16%), extramedullary haematopoiesis (12%) and splenitis (8%). A honeycomb pattern was successfully identified with a linear high-frequency probe in all cats, but only in 36% of cases with the micro-convex probe. Follow-up information was available for four cats, in which the honeycomb appearance persisted up to 105 days after the first examination; there was persistence of the honeycomb pattern in all cases. Cats with a splenic cytological diagnosis of extramedullary haematopoiesis had the lowest haemoglobin plasma concentration ( P = 0.011). Conclusions and relevance Honeycomb appearance of the spleen is uncommon in cats and, in our study, was systematically associated with cytological alterations; most of the time it was benign (84%). The use of a high-frequency linear probe improves its detection rate. No epidemiological, ultrasonographic or clinical criteria allow differentiation between the different types of infiltration and fine-needle aspiration is therefore recommended.


2020 ◽  
Vol 11 (e) ◽  
pp. e183.1-e183.3
Author(s):  
Sridhar Swetha ◽  
Samayam Aneesh ◽  
Anjan Kumar Patra

Keratoderma hereditarium mutilans or Vohwinkel’s syndrome is a rare autosomal dominant type of palmoplantar keratoderma characterized by honeycomb appearance, pseudoainhum leading to auto-amputation and stellate keratosis on knuckles. It’s mode of inheritance is autosomal dominant with mutation in loricrin and connexin 26 genes. We report the case of a 35-year-old female with alopecia universalis since birth and transgradient palmoplantar keratoderma, impaired hearing and pseudoainhum formation since childhood. This case is being reported to highlight the association of Vohwinkel’s syndrome with sensorineural hearing loss and alopecia universalis.


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