19 results on '"Sastrowijoto, S. H."'
Search Results
2. Mutations in the heparan sulfate backbone elongating enzymes EXT1 and EXT2 have no major effect on endothelial glycocalyx and the glomerular filtration barrier
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Khalil, Ramzi, Boels, Margien G. S., Bezuijen, A., Boers, J. E., de Bruin, P. C., van Dijk, M. A. A. M., Drillenburg, P., Hamel, A. F., Hazelbag, H. M., Jonges, G. N., Kibbelaar, R. E., Lam, K. H., van der Linden, H., van Marsdijk, J., Meijer, C., Nagtegaal, I. D., Oudejans, J. J., Roelofs, J. J. T. H., Rozendaal, L., Sastrowijoto, S. H., Smits, M. M., Stavast, J., van den Berg, Bernard M., Bruijn, Jan A., Rabelink, Ton J., Hogendoorn, Pancras C. W., Baelde, Hans J., Neurology, Pathology, Internal medicine, ACS - Diabetes & metabolism, and ACS - Pulmonary hypertension & thrombosis
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Hereditary multiple exostosis ,General Medicine ,Multiple osteochondromas ,N-Acetylglucosaminyltransferases ,Glycocalyx ,Bone neoplasm ,urologic and male genital diseases ,Glomerular filtration barrier ,Proteinuria ,Mutation ,Genetics ,Tumours of the digestive tract Radboud Institute for Molecular Life Sciences [Radboudumc 14] ,Humans ,Albuminuria ,Heparitin Sulfate ,Endothelium ,Molecular Biology - Abstract
In this study, the effect of heterozygous germline mutations in the heparan sulfate (HS) glycosaminoglycan chain co-polymerases EXT1 and EXT2 on glomerular barrier function and the endothelial glycocalyx in humans is investigated. Heparan sulfate (HS) glycosaminoglycans are deemed essential to the glomerular filtration barrier, including the glomerular endothelial glycocalyx. Animal studies have shown that loss of HS results in a thinner glycocalyx. Also, decreased glomerular HS expression is observed in various proteinuric renal diseases in humans. A case report of a patient with an EXT1 mutation indicated that this could result in a specific renal phenotype. This patient suffered from multiple osteochondromas, an autosomal dominant disease caused by mono-allelic germline mutations in the EXT1 or EXT2 gene. These studies imply that HS is indeed essential to the glomerular filtration barrier. However, loss of HS did not lead to proteinuria in various animal models. We demonstrate that multiple osteochondroma patients do not have more microalbuminuria or altered glycocalyx properties compared to age-matched controls (n = 19). A search for all Dutch patients registered with both osteochondroma and kidney biopsy (n = 39) showed that an EXT1 or EXT2 mutation does not necessarily lead to specific glomerular morphological phenotypic changes. In conclusion, this study shows that a heterozygous mutation in the HS backbone elongating enzymes EXT1 and EXT2 in humans does not result in (micro)albuminuria, a specific renal phenotype or changes to the endothelial glycocalyx, adding to the growing knowledge on the role of EXT1 and EXT2 genes in pathophysiology.
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- 2022
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3. Better survival of renal cell carcinoma in patients with inflammatory bowel disease
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Derikx, Lauranne A. A. P., Nissen, Loes H. C., Drenth, Joost P. H., van Herpen, Carla M., Kievit, Wietske, Verhoeven, Rob H. A., Mulders, Peter F. A., Hulsbergen-van de Kaa, Christina A., Boers-Sonderen, Marye J., van den Heuvel, Tim R. A., Pierik, Marieke, Nagtegaal, Iris D., Hoentjen, Frank, Kluin, P. M., Hogenes, M., Hamel, A. F., Natté, R., van Dijk, C. M., Kusters-Vandevelde, H. V. N., Sastrowijoto, S. H., Willig, A. P., Dijkstra, G., van der Meulen-de Jong, A. E., Vu, M. K., Cats, A., Haanen, J. B. A. G., van der Woude, C. J., Russel, M. G. V. M., Oldenburg, B., Meeuse, J. J., Corporaal, S., Zonneveld, A. M., Wahab, P. J., van den Hazel, S. J., Mares, W. G. N., Lieverse, R. J., Meijssen, M. A. C., Thuernau, K., Janik, D., van der Heide, H., Ponsioen, C. Y., Stokkers, P. C. F., Gastroenterology and Hepatology, Interne Geneeskunde, and RS: NUTRIM - R2 - Gut-liver homeostasis
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Male ,Time Factors ,Kaplan-Meier Estimate ,urologic and male genital diseases ,Inflammatory bowel disease ,Crohn Disease ,Risk Factors ,Renal cell carcinoma ,Odds Ratio ,Tumours of the digestive tract Radboud Institute for Molecular Life Sciences [Radboudumc 14] ,Medicine ,Registries ,Early Detection of Cancer ,Netherlands ,Aged, 80 and over ,education.field_of_study ,Age Factors ,Middle Aged ,Prognosis ,Kidney Neoplasms ,female genital diseases and pregnancy complications ,Oncology ,Cohort ,Female ,medicine.symptom ,Immunosuppressive Agents ,Inflammatory diseases Radboud Institute for Molecular Life Sciences [Radboudumc 5] ,Rare cancers Radboud Institute for Health Sciences [Radboudumc 9] ,Adult ,renal cell carcinoma ,Pancolitis ,medicine.medical_specialty ,Population ,immunosuppressive therapy ,Risk Assessment ,Immunocompromised Host ,Predictive Value of Tests ,inflammatory bowel disease ,Internal medicine ,Urological cancers Radboud Institute for Molecular Life Sciences [Radboudumc 15] ,Humans ,education ,Carcinoma, Renal Cell ,Aged ,Proportional Hazards Models ,Retrospective Studies ,Chi-Square Distribution ,Tumor Necrosis Factor-alpha ,business.industry ,Retrospective cohort study ,Odds ratio ,medicine.disease ,digestive system diseases ,Surgery ,Cancer registry ,Renal disorders Radboud Institute for Molecular Life Sciences [Radboudumc 11] ,Multivariate Analysis ,Inflammatory diseases Radboud Institute for Health Sciences [Radboudumc 5] ,Colitis, Ulcerative ,Clinical Research Paper ,business - Abstract
// Lauranne A.A.P. Derikx 1 , Loes H.C. Nissen 1 , Joost P.H. Drenth 1 , Carla M. van Herpen 2 , Wietske Kievit 3 , Rob H.A. Verhoeven 4 , Peter F.A. Mulders 5 , Christina A. Hulsbergen-van de Kaa 6 , Marye J. Boers-Sonderen 2 , Tim R.A. van den Heuvel 7 , Marieke Pierik 7 , Iris D. Nagtegaal 6 , Frank Hoentjen 1 , On behalf of the Dutch Initiative on Crohn and Colitis (ICC), PALGA group and IBD/RCC group 1 Inflammatory Bowel Disease Centre, Department of Gastroenterology and Hepatology, Radboud university medical centre, Nijmegen, The Netherlands 2 Department of Medical Oncology, Radboud university medical centre, Nijmegen, The Netherlands 3 Radboud Institute for Health Sciences, Radboud university medical centre, Nijmegen, The Netherlands 4 Netherlands comprehensive cancer organization / Netherlands Cancer Registry, Utrecht, The Netherlands 5 Department of Urology, Radboud university medical centre, Nijmegen, The Netherlands 6 Department of Pathology, Radboud university medical centre, Nijmegen, The Netherlands 7 Department of Gastroenterology and Hepatology, Maastricht University Medical Centre, Maastricht, The Netherlands Correspondence to: Lauranne A.A.P. Derikx, e-mail: Lauranne.Derikx@radboudumc.nl Keywords: inflammatory bowel disease, renal cell carcinoma, immunosuppressive therapy Received: June 30, 2015 Accepted: September 24, 2015 Published: October 05, 2015 ABSTRACT Background: Immunosuppressive therapy may impact cancer risk in inflammatory bowel disease (IBD). Cancer specific data regarding risk and outcome are scarce and data for renal cell carcinoma (RCC) are lacking. We aimed(1) to identify risk factors for RCC development in IBD patients (2) to compare RCC characteristics, outcome and survival between IBD patients and the general population. Methods: A PALGA (Dutch Pathology Registry) search was performed to establish a case group consisting of all IBD patients with incident RCC in The Netherlands (1991–2013). Cases were compared with two separate control groups: (A) with a population-based IBD cohort for identification of risk factors (B) with a RCC cohort from the general population to compare RCC characteristics and outcomes. Results: 180 IBD patients with RCC were identified. Pancolitis (OR 1.8–2.5), penetrating Crohn’s disease (OR 2.8), IBD related surgery (OR 3.7–4.5), male gender (OR 3.2–5.0) and older age at IBD onset (OR 1.0–1.1) were identified as independent risk factors for RCC development. IBD patients had a significantly lower age at RCC diagnosis ( p < 0.001), lower N-stage ( p = 0.025), lower M-stage ( p = 0.020) and underwent more frequently surgical treatment for RCC ( p < 0.001) compared to the general population. This translated into a better survival ( p = 0.026; HR 0.7) independent of immunosuppression. Conclusions: IBD patients with a complex phenotype are at increased risk to develop RCC. They are diagnosed with RCC at a younger age and at an earlier disease stage compared to the general population. This translates into a better survival independent of immunosuppressive or anti-TNFα therapy.
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- 2015
4. Tumoral calcinosis.
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Smeets, H G, primary, Lamers, R J, additional, and Sastrowijoto, S H, additional
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- 1996
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5. Improved metabolic control, clinical periodontal status and subgingival microbiology in insulin-dependent diabetes mellitus.
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Sastrowijoto, S. H., primary, Velden, U., additional, Steenbergen, T. J. M., additional, Hillemans, P., additional, Hart, A. A. M., additional, Graaff, J., additional, and Abraham-lnpijn, L., additional
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- 1992
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6. Relationship between bleeding/ plaque ratio, family history of diabetes mellitus and impaired glucose tolerance
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Sastrowijoto, S. H., primary, Abbas, F., additional, Abraham-lnpijn, L., additional, and Velden, U., additional
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- 1992
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7. Improved metabolic control, clinical periodontal status and subgingival microbiology in insulin‐dependent diabetes mellitus
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Sastrowijoto, S. H., primary, van der Velden, U., additional, van Steenbergen, T. J. M., additional, Hillemans, P., additional, Hart, A. A. M., additional, de Graaff, J., additional, and Abraham‐Inpijn, L., additional
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- 1990
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8. Relationship between bleeding/plaque ratio, family history of diabetes mellitus and impaired glucose tolerance
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Sastrowijoto, S. H., primary, Abbas, F., additional, Abraham-lnpijn, L., additional, and Velden, U., additional
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- 1990
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9. Periodontal condition and microbiology of healthy and diseased periodontal pockets in type 1 diabetes mellitus patients.
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Sastrowijoto, S. H., Hillemans, P., van Steenbergen, T. J. M., Abraham-Inpijn, L., and Graaff, J. de
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METABOLIC regulation , *BLOOD proteins , *HYPOGLYCEMIC agents , *ENDOCRINE diseases , *PATHOGENIC microorganisms , *PEOPLE with diabetes , *BACTEROIDES - Abstract
On the basis of glycosylated hemoglobin (HbA1c) values, 22 type 1 (insulin-dependent) diabetic adults were grouped into patients with near normal (HbA1c≤7.7%) and poor (HbA1c≥9.9%) metabolic control. A total of 44 subgingival sites were examined for Actinobacillus actinomycetemcomitans, black-pigmented Bacteroides species and Capnocytophaga species. No significant difference could be demonstrated between patients in the 2 test groups with regard to periodontal condition. Neither age of diabetic patients nor duration of diabetes mellitus influenced the periodontal parameters. In both test groups, pocket depth of 4 mm or more (≥4 mm) was found to be significantly associated with increased swelling, bleeding after probing and amount of marginal plaque. Proportionally high %s of cultivable A. actinomycetemcomitans (mean 4.3%; range 2.8-5.8%), Bacteroides gingivalis (33.2% and 34.6%) and Bacteroides intermedius (mean 4.2%; range 0.001-13.5%) were isolated from diseased periodontal pockets. In diabetic patients with poor metabolic control, B. intermedius was isolated from diseased periodontal pockets with a mean % of 7.2%, range 0.3-12.5%. Independent of the degree of metabolic control, low %s of Capnocytophaga species were isolated from diseased and healthy periodontal pockets, mean 0.9% (range 0.003-3.9%) and mean 1.4% (range 0.04-4.9%), respectively. It was concluded from this study that metabolic control seems to have no direct effect on the periodontium. Furthermore, the role of Capnocytophaga species in the pathogenesis of infectious periodontal disease in type 1 diabetic patients seems to be overestimated. However A. actinomycetemcomitans and blackpigmented Bacteroides species may be important pathogens in periodontal disease in type 1 diabetic patients, as they are known to be in non-diabetic periodontal patients. [ABSTRACT FROM AUTHOR]
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- 1989
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10. [A cecum carcinoma and liver and peritoneal lesions].
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Moossdorff M, Sastrowijoto SH, Sosef MN, and de Witte E
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- Abdominal Pain etiology, Adult, Cecal Neoplasms complications, Cecum pathology, Colectomy, Humans, Liver pathology, Male, Peritoneum pathology, Tomography, X-Ray Computed, Carcinoma secondary, Cecal Neoplasms pathology, Liver Neoplasms secondary, Peritoneal Neoplasms secondary
- Abstract
A 37-year-old male presented with acute lower right abdominal pain. A CT-scan showed a cecal mass. During laparoscopic right colectomy, multiple liver lesions and peritoneal deposits were seen. Histology confirmed pT4aN0 cecum carcinoma, but the liver lesions were consistent with sarcoidosis, and the peritoneal deposits were suggestive of benign mesothelioma.
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- 2021
11. Analysis of local recurrence after breast conservative treatment for invasive breast cancer: a single institution cohort.
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Pomp J, Blom J, Zwinderman AH, Sastrowijoto SH, and van Krimpen C
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- Age of Onset, Biomarkers, Tumor, Cohort Studies, Female, Humans, Middle Aged, Prognosis, Risk Factors, Treatment Outcome, Breast Neoplasms pathology, Breast Neoplasms surgery, Mastectomy, Segmental, Neoplasm Recurrence, Local, Neoplasm Staging
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In a group of 900 patients treated for carcinoma of the breast, we evaluated patient-, tumour- and treatment-related parameters, predicting the success or failure of conservative treatment for invasive breast cancer. Thirty-one patients developed local recurrences which were detected within 0.1-12.1 years after treatment of the primary tumour (with a median of 6.2 years), providing a risk of 2% at 5 years and 9% at 10 years. The locally recurrent tumours and their original primary tumours of 28 patients could be retrieved from the pathology laboratory archives. These 28 tumours of the recurrence group (RG) were matched with tumours without local recurrence, the non-recurrence group, for age at time of diagnosis, duration of follow-up and T- and N-stage. The tumours were studied for type and grade of invasive tumour including the in situ component and involvement of surgical margins. In addition, the expression of cell-cycle proteins, p53, Ki-67 (MIB-1) and BCL-1, as well as HER-2/ neu oncoprotein, estrogen and progesterone receptor were investigated. We found a mean age at diagnosis for the RG of 50 years, and the mean age at time of diagnosis for the whole group of 900 patients was 56 years (p=0.003). Thirty-nine percent of the RG had a positive surgical margin, which was the case for only 18% in the control group (p=0.09). The presence of the in situ component was also correlated with increased local recurrence (p=0.022). Furthermore, local recurrence was also associated with a significantly increased occurrence of distant metastases (p=0.001). We conclude that breast conservative treatment is safe with a low local recurrence rate.
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- 2005
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12. [Diagnostic image (152). A man with a swelling in the groin. Malignant eccrine poroma].
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Keijzer R, Sastrowijoto SH, Brakman M, and van der Elst M
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- Acrospiroma pathology, Acrospiroma surgery, Aged, Eccrine Glands pathology, Groin, Humans, Male, Sweat Gland Neoplasms pathology, Sweat Gland Neoplasms surgery, Acrospiroma diagnosis, Sweat Gland Neoplasms diagnosis
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A malignant eccrine poroma (porocarcinoma) was excised from the right groin of a 78-year-old man.
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- 2003
13. [Recurrent otitis media and mastoiditis due to atypical mycobacteria].
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Vreede RW, Kruyt JM, Nijhuis-Heddes JM, and Sastrowijoto SH
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- Anti-Bacterial Agents therapeutic use, Child, Diagnosis, Differential, Female, Humans, Mycobacterium Infections, Nontuberculous drug therapy, Recurrence, Mastoiditis microbiology, Mycobacterium Infections, Nontuberculous diagnosis, Mycobacterium chelonae isolation & purification, Otitis Media with Effusion microbiology
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An eleven-year-old girl was operated on due to right-sided chronic otitis media with effusion. After three months, an impressive enlargement of the mucosal lining developed, for which thorough debridement of the middle ear and mastoid was performed. Histological examination revealed a granulomatous inflammation, with negative Ziehl-Neelsen staining. Standard bacteriological cultures revealed no pathogenic micro-organisms. Three weeks later the same clinical picture developed, once again followed by extensive surgical debridement. After a thorough diagnostic work-up an atypical mycobacterium was found, namely Mycobacterium abscessus--formerly named M. chelonei subspecies abscessus. Following appropriate antibiotic therapy the patient was symptom-free. Mycobacterial infections should be part of the differential diagnosis of persistent otorrhoea.
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- 2002
14. [Less operations required due to perioperative frozen section examination of sentinel nodes in 275 breast cancer patients].
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van der Loo EM, Sastrowijoto SH, Bril H, van Krimpen C, de Graaf PW, and Eulderink F
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- Aged, Carcinoma pathology, Carcinoma secondary, Female, Humans, Lymphatic Metastasis pathology, Mastectomy methods, Middle Aged, Reoperation statistics & numerical data, Retrospective Studies, Treatment Outcome, Breast Neoplasms diagnosis, Breast Neoplasms surgery, Carcinoma diagnosis, Carcinoma surgery, Sentinel Lymph Node Biopsy statistics & numerical data
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Objective: To determine the reliability of a peroperative frozen section examinations of sentinel lymph nodes in mammary carcinoma., Design: Retrospective., Method: In the Reinier de Graaf Hospital and Diagnostic Centre SSDZ Delft, the Netherlands, the results of frozen section from sentinel lymph node investigations of mammary carcinomas from 1997-2000 were compared with the final pathological results. If axillary dissection had been performed on these patients, the histopathological findings of the dissected lymph nodes were also studied., Results: Frozen sections were made of 287 sentinel lymph nodes from 275 patients. A tumour was found in the sentinel lymph nodes of 64 patients and these patients immediately underwent a complete axillary lymph node dissection. For 31 of these patients a tumour was also found in the other lymph nodes. In 29 of these 31 patients, histological examination had shown extranodal extension. The frozen sections from the sentinel nodes of the remaining 211 patients were considered negative. However, in 13 of these patients, the paraffin sections of the sentinel node nevertheless showed a tumour and the remaining axillary lymph nodes were removed in a second operation. In the last 89 patients studied, the sentinel lymph nodes were cut at four levels and stained immunohistochemically at one level for cytokeratins. Accordingly micrometastases were found in the sentinel lymph nodes of 4 of the 13 patients with (false-)negative frozen sections. False-positive results did not occur., Conclusion: The major advantage of the sentinel node method in breast cancer is that for women without metastasis present in the sentinel node, axillary dissection is avoided. By means of a peroperative examination of frozen sections, 83% of the patients with a metastasis in the sentinel lymph node (or about one quarter of all patients) were spared from having a second operation for axillary dissection at a later stage.
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- 2001
15. Lethal hypophosphatasia, spur type: case report and fetopathological study.
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Vandevijver N, De Die-Smulders CE, Offermans JP, Van Der Linden ES, Arends JW, Sastrowijoto SH, Moerman P, and Fryns JP
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- Adult, Consanguinity, Diagnosis, Differential, Fatal Outcome, Female, Fetal Death, Fetus diagnostic imaging, Fetus pathology, Gestational Age, Humans, Pregnancy, Radiography, Fetal Diseases pathology, Hypophosphatasia pathology
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Lethal hypophosphatasia, spur type: case report and fetopathological study: Hypophosphatasia (HP) is characterised by severe undermineralisation of the skeleton owing to deficiency of tissue nonspecific alkaline phosphatase. Clinically a perinatal, infantile, childhood and adult type is distinguished. Clinical signs in the perinatal type of HP show considerable overlap with other skeletal dysplasias such as osteogenesis imperfecta type IIA and type IIC, and achondrogenesis type IA. If present, "spurs" of the limbs are diagnostic for HP. We present a prenatally diagnosed case of HP and discuss the differential diagnosis based on clinical, radiological and pathological findings. Our findings indicate that two types of spurs can be distinguished in hypophosphatasia: midshaft type and joint type.
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- 1998
16. Tumoral calcinosis.
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Smeets HG, Lamers RJ, and Sastrowijoto SH
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- Adult, Hip, Humans, Kidney Transplantation, Magnetic Resonance Imaging, Male, Calcinosis diagnosis, Muscular Diseases diagnosis
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- 1996
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17. Prenatal ultrasound diagnosis of rhizomelic chondrodysplasia punctata in a primigravida.
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Sastrowijoto SH, Vandenberghe K, Moerman P, Lauweryns JM, and Fryns JP
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- Adult, Chondrodysplasia Punctata complications, Female, Femur abnormalities, Fetal Diseases diagnostic imaging, Gestational Age, Heart Defects, Congenital complications, Heart Defects, Congenital pathology, Humans, Humerus abnormalities, Liver abnormalities, Male, Pregnancy, Thymus Gland pathology, Chondrodysplasia Punctata diagnostic imaging, Ultrasonography, Prenatal
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Rhizomelic chondrodysplasia punctata (RCDP) is a sublethal autosomal recessive disorder characterized by skeletal dysplasia, microcephaly, mental retardation, congenital cataracts, joint contractures, skin changes, and failure to thrive. Prenatal ultrasound diagnosis has been reported during the second trimester of pregnancy. Prenatal diagnosis is also possible from the first trimester onwards by demonstration of peroxisomal dysfunction in cultured chorionic villous or amniotic fluid cells. In all cases reported hitherto, the prenatal diagnosis was established after the birth of a previous affected child. In contrast to these studies in pregnant multiparous women at risk for RCDP, we report on the first case of prenatal ultrasound diagnosis of RCDP at 19 weeks' gestation in a primigravida. In addition, a complex cardiac malformation associated with hypoplasia of the thymus (DiGeorge anomaly) is described.
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- 1994
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18. Hereditary renal adysplasia: new observations and hypotheses.
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Moerman P, Fryns JP, Sastrowijoto SH, Vandenberghe K, and Lauweryns JM
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- Abnormalities, Multiple, Amniotic Fluid cytology, Cells, Cultured, Chromosomes, Human, Pair 6, Female, Fetal Death, Fetal Diseases genetics, Fetal Diseases pathology, Fibroblasts pathology, Gestational Age, Humans, Infant, Newborn, Karyotyping, Male, Polycystic Kidney, Autosomal Dominant pathology, Translocation, Genetic genetics, Kidney abnormalities, Polycystic Kidney, Autosomal Dominant genetics
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Renal agenesis and dysplasia are frequently regarded by pathologists, even pediatric pathologists, as sporadic malformations. We report six fetal autopsy cases of hereditary renal adysplasia (HRA): two pairs of siblings, one case with paternal unilateral renal agenesis, and one case with an autosomal balanced 6p/19q translocation. The main purpose of this paper is to emphasize that nonsyndromal renal agenesis and dysplasia are pathogenetically related and often inherited as an autosomal dominant trait with incomplete penetrance and variable expression. A subsidiary purpose is to present a case of bilateral multicystic dysplasia with a balanced 6p/19q translocation. This observation further supports the assignment of one of the loci for HRA to chromosome 6p.
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- 1994
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19. An unusual case of black teeth.
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Schuurs AH, Abraham-Inpijn L, van Straalen JP, and Sastrowijoto SH
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- Adult, Bacteroides isolation & purification, Capsicum, Dentin pathology, Humans, Male, Plants, Medicinal, Saliva physiology, Staphylococcus epidermidis isolation & purification, Tooth Abrasion complications, Tooth Discoloration microbiology, Tooth Discoloration pathology, Tooth Erosion complications, Wine adverse effects, Tooth Discoloration etiology
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Loss of enamel and a deep black stain of the teeth in a 40-year-old diabetic patient are strongly suggested to be caused by the daily consumption of a cheap white wine and, possibly, by the chewing of cayenne. The wine proved to be rather acid, thereby promoting abrasion as a result of gnashing, and to contain a high concentration of tannin. The exact role of the tannins is described.
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- 1987
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