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Dive into the research topics where Sam Ghazi is active.

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Featured researches published by Sam Ghazi.


Journal of Perinatal Medicine | 2008

Correlation between ultrasound and autopsy findings after 2nd trimester terminations of pregnancy.

Per Antonsson; Anders Sundberg; Marius Kublickas; Christina Pilo; Sam Ghazi; Magnus Westgren; Nikos Papadogiannakis

Abstract Objective: To compare ultrasound (US) and fetal autopsy findings in 2nd trimester termination of pregnancy because of structural fetal anomalies. Methods: A total of 112 terminations of pregnancy (TOP) between 1999–2003 were reviewed retrospectively. The cases originated from a secondary and a tertiary Fetal Medicine unit in the south Stockholm area, using a common specialized perinatal pathology service. Karyotype was not known at the time of US examination. The findings were compared and classified into four groups according to the degree of agreement between US and autopsy. Results: In 45% of cases there was total agreement between US and autopsy. In 40%, autopsy confirmed all US findings but provided additional information of clinical importance. Partial or total lack of agreement was noted in 11% and 4% of the cases, respectively. Areas of discrepancy involved mainly CNS- and cardiovascular abnormalities and, to a lesser extent, renal anomalies, abdominal wall defects and hydrops/hygroma. Regarding CNS abnormalities the overall rate of agreement was 62%; it was highest in acrania/anencephaly (92%) and lowest in hydrocephaly (39%). Conclusion: We find an overall high degree of agreement between US and autopsy findings. Autopsy often provided additional information of clinical value and it should always follow US examination and TOP. Fixation of CNS is crucial for optimal results. Specific limitations of autopsy, i.e., detection of CNS abnormalities, may be reduced by complementary imaging techniques, such as MRI. The ability of US to detect cardiac anomalies is enhanced with the close contact to specialized fetal cardiology.


World Journal of Surgical Oncology | 2013

Clinicopathological analysis of colorectal cancer: a comparison between emergency and elective surgical cases

Sam Ghazi; Elisabeth Berg; Annika Lindblom; Ulrik Lindforss

BackgroundApproximately 15 to 30% of colorectal cancers present as an emergency, most often as obstruction or perforation. Studies report poorer outcome for patients who undergo emergency compared with elective surgery, both for their initial hospital stay and their long-term survival. Advanced tumor pathology and tumors with unfavorable histologic features may provide the basis for the difference in outcome. The aim of this study was to compare the clinical and pathologic profiles of emergency and elective surgical cases for colorectal cancer, and relate these to gender, age group, tumor location, and family history of the disease. The main outcome measure was the difference in morphology between elective and emergency surgical cases.MethodsIn total, 976 tumors from patients treated surgically for colorectal cancer between 2004 and 2006 in Stockholm County, Sweden (8 hospitals) were analyzed in the study. Seventeen morphological features were examined and compared with type of operation (elective or emergency), gender, age, tumor location, and family history of colorectal cancer by re-evaluating the histopathologic features of the tumors.ResultsIn a univariate analysis, the following characteristics were found more frequently in emergency compared with elective cases: multiple tumors, higher American Joint Committee on Cancer (AJCC), tumor (T) and node (N) stage, peri-tumor lymphocytic reaction, high number of tumor-infiltrating lymphocytes, signet-ring cell mucinous carcinoma, desmoplastic stromal reaction, vascular and perineural invasion, and infiltrative tumor margin (P<0.0001 for AJCC stage III to IV, N stage 1 to 2/3, and vascular invasion). In a multivariate analysis, all these differences, with the exception of peri-tumor lymphocytic reaction, remained significant (P<0.0001 for multiple tumors, perineural invasion, infiltrative tumor margin, AJCC stage III, and N stage 1 to 2/3).ConclusionsColorectal cancers that need surgery as an emergency case generally show a more aggressive histopathologic profile and a more advanced stage than do elective cases. Essentially, no difference was seen in location, and therefore it is likely there would be no differences in macro-environment either. Our results could indicate that colorectal cancers needing emergency surgery belong to an inherently specific group with a different etiologic or genetic background.


Pediatric and Developmental Pathology | 2010

The Number of CD68+ (Hofbauer) Cells is Decreased in Placentas with Chorioamnionitis and with Advancing Gestational Age

Marie-Therese Vinnars; Erika Rindsjö; Sam Ghazi; Anders Sundberg; Nikos Papadogiannakis

Hofbauer cells are placental macrophages found in chorionic villous stroma; they express classic monocyte/macrophage markers, such as CD68. Little is known about their participation in placental disease and immunologic interactions at the placental interface. The aim of this study was to quantify the amount of Hofbauer cells in placentas complicated, or not, by chorioamnionitis and in placentas from different gestational ages. Fifty-eight 2nd-and 3rd-trimester placentas with the histologic diagnosis of acute chorioamnionitis were compared with 42 control placentas matched according to gestational age. Immunohistochemistry evaluation was performed with a monoclonal anti-CD68 antibody. Five areas of each placenta were photographed and 5 investigators, with the help of a computerized image analysis program, independently evaluated the number of CD68+ cells. Our results showed that there are significantly fewer CD68+ cells per villous area in placentas diagnosed with chorioamnionitis than in those of controls (P < 0.001). Moreover, there was a significant overall decrease in the number of these cells in 3rd as compared with 2nd trimester placentas (P = 0.02), as well as in placentas from term as compared to preterm pregnancies (P = 0.004). Our data indicate that CD68+ Hofbauer cells may be involved in placental infection and possibly associated with the developmental maturation of the fetoplacental unit.


European Journal of Gastroenterology & Hepatology | 2009

Severe liver damage associated with celiac disease: findings in six toddler-aged girls.

Thomas Casswall; Nikos Papadogiannakis; Sam Ghazi; Antal Nemeth

Objective Light-to-moderate liver damage is often seen in children diagnosed with celiac disease, but severe liver damage is rarely observed. Methods During a 12-year-long period our center took care of six 13–36-month-old girls who developed severe liver damage 1–24 months after the diagnosis of celiac disease. Results Four girls had acute liver failure; two of them had to be liver transplanted. The other four girls recovered without transplantation and none of the six patients developed autoimmune disease during the 2–14-year-long follow-up period. Although adenovirus type 2 was found in the urine and stools of one girl, her liver histopathology did not resemble viral hepatitis. Certain autoimmune features could be observed initially in some of the children but finally none of them fulfilled the criteria for autoimmune liver disease and this pattern did not change during the several years of follow-up. Thorough investigation could not find any alternative pathogenetic cause and thus, the association with celiac disease is obvious. Histopathology showed various degrees of intralobular inflammation, necrosis, involvement of the small bile ducts, and in one case interface hepatitis; but in general, histopathology did not reveal a common pathogenetic mechanism. Conclusion Although rare, severe hepatic damage or failure can develop in association with celiac disease. The etiology is varying and multifactorial. Consequently, children with newly onset celiac disease should be routinely checked for liver function and vice versa, children with severe liver damage should be investigated for untreated celiac disease.


American Journal of Pathology | 2010

Colorectal Cancer Susceptibility Loci in a Population-Based Study : Associations with Morphological Parameters

Sam Ghazi; Susanna von Holst; Simone Picelli; Ulrik Lindforss; Albert Tenesa; Susan M. Farrington; Harry Campbell; Malcolm G. Dunlop; Nikos Papadogiannakis; Annika Lindblom

Recent genome-wide association studies have identified multiple genetic loci and single nucleotide polymorphisms (SNPs) associated with either increased or decreased risk of colorectal cancer (CRC). In the present study, our objective was to determine whether 11 of the new susceptibility CRC loci are associated with tumor morphology and to confirm these loci as distinct and etiologically different risk factors in the development of CRC. The following clinical and morphological parameters were analyzed in 1572 samples: tumor size, T-stage, lymph node metastases, degree of differentiation, mucin production, Crohn-like peritumoral lymphocytic infiltration, tumor-infiltrating lymphocytes, desmoplastic reaction, necrosis, invasion of blood or lymph vessels, perineural growth, medullary type, budding, and tumor margin. One SNP from each of the 11 loci (rs6983267 on 8q24.21, rs16892766 on 8q23.3, rs719725 on 9p24.1, rs10795668 on 10p14, rs3802842 on 11q23.1, rs4444235 on 14q22.2, rs4779584 on 15q13.3, rs9929218 on 16q22.1, rs4939827 on 18q21.1, rs10411210 on 19q13.11, and rs961253 on 20p12.3) was genotyped for all cases. Odds ratios, 95% confidence intervals, and the corresponding P values were calculated for the 11 SNPs identified above. A cross tabulation between SNPs and morphology was performed. Several loci showed statistically significant associations with specific phenotypes. The findings are consistent with pathogenic variants in several loci that act in distinct CRC and morphogenetic pathways. Further large-scale studies are required to validate these findings.


Pediatric and Developmental Pathology | 2012

Development of fetal intestinal length during 2nd-trimester in normal and pathologic pregnancies.

Andreas Marnerides; Sam Ghazi; Anders Sundberg; Nikos Papadogiannakis

Linear growth of the human fetal gastrointestinal tract is not often discussed in the literature, and little is known about the effects of chromosomal abnormalities and intrauterine growth restriction (IUGR) on intestinal length, especially during the 2nd trimester. Accurate evaluation of intestinal length and knowledge of normal and reference values are of clinical importance. For example, intestinal resection may be necessary in preterm infants with necrotizing enterocolitis or mid-gut volvulus, and the surgeon should use data to be judicious in the amount removed. Linear measurements are essential in evaluating fetal development ultrasonographically and are an integral part of the postmortem examination. The intestinal lengths of 203 2nd-trimester fetuses and premature infants were measured. Small intestine length (SIL), colon length (CL), total bowel length (TBL; TBL = SIL + CL), and the length of the appendix (AL) increased with gestational age. No differences between the genders were observed. Colon length increased secondary to maceration, but no such effects were shown on SIL, TBL, or AL. No differences were shown in relation to IUGR. Small intestine length, CL, and TBL, but not AL, were shorter in fetuses with trisomy 21. Appendix length was not affected by any of the studied factors. We propose that the measurement of the length of the appendix may be used as an additional parameter for the postmortem evaluation of gestational age. Furthermore, its assessment may have potential as an ultrasonographic indicator of gestational age, particularly for the 2nd trimester.


Journal of Immunotherapy | 2017

A Preliminary Report: Radical Surgery and Stem Cell Transplantation for the Treatment of Patients With Pancreatic Cancer

Brigitta Omazic; Burcu Ayoglu; Matthias Löhr; Ralf Segersvärd; Caroline S. Verbeke; Isabelle Magalhaes; Zuzana Potácová; Jonas Mattsson; Alexei Terman; Sam Ghazi; Nils Albiin; Nikolaos Kartalis; Peter Nilsson; Thomas Poiret; Liu Zhenjiang; Rainer Heuchel; Jochen M. Schwenk; Johan Permert; Markus Maeurer; Olle Ringdén

We examined the immunologic effects of allogeneic hematopoietic stem cell transplantation (HSCT) in the treatment of pancreatic ductal adenocarcinoma, a deadly disease with a median survival of 24 months for resected tumors and a 5-year survival rate of 6%. After adjuvant chemotherapy, 2 patients with resected pancreatic ductal adenocarcinoma underwent HSCT with HLA-identical sibling donors. Comparable patients who underwent radical surgery, but did not have a donor, served as controls (n=6). Both patients developed humoral and cellular (ie, HLA-A*01:01-restricted) immune responses directed against 2 novel tumor-associated antigens (TAAs), INO80E and UCLH3 after HSCT. Both TAAs were highly expressed in the original tumor tissue suggesting that HSCT promoted a clinically relevant, long-lasting cellular immune response. In contrast to untreated controls, who succumbed to progressive disease, both patients are tumor-free 9 years after diagnosis. Radical surgery combined with HSCT may cure pancreatic adenocarcinoma and change the cellular immune repertoire capable of responding to clinically and biologically relevant TAAs.


The Forum | 2018

Ein Fall von Pankreaskarzinom

J.-Matthias Löhr; Maximilian Kordes; Maria Gustafsson-Liljefors; Sam Ghazi; Nikolaos Kartalis; Valtteri Wirta; Jan-Eric Frödin; Thilo Hackert; Stephan Brock; Katrin Stecker; Caroline Huelsewig; Lars Ernstrand; Johan Permert; Dirk Jäger

FORUM 2018 · 33:232–235 https://doi.org/10.1007/s12312-018-0458-4 Online publiziert: 14. August 2018


Journal of Gastroenterology | 2012

Analysis of colorectal cancer morphology in relation to sex, age, location, and family history.

Sam Ghazi; Ulrik Lindforss; Greger Lindberg; Elisabeth Berg; Annika Lindblom; Nikos Papadogiannakis


Anticancer Research | 2017

Defining New Colorectal Cancer Syndromes in a Population-based Cohort of the Disease

Anna Forsberg; Anne Keränen; Susanna von Holst; Simone Picelli; Nikos Papadogiannakis; Sam Ghazi; Annika Lindblom

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Nikos Papadogiannakis

Karolinska University Hospital

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Annika Lindblom

Karolinska University Hospital

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Ulrik Lindforss

Karolinska University Hospital

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Anders Sundberg

Karolinska University Hospital

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Johan Permert

Karolinska University Hospital

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Nikolaos Kartalis

Karolinska University Hospital

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Greger Lindberg

Karolinska University Hospital

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J.-Matthias Löhr

Karolinska University Hospital

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