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12 results on '"C. Verhelst"'

1. Longitudinal profiles of resting energy metabolism of adult covid-19 patients in intensive care

Author

C. Verhelst, J. Demol, J. Geers, E. De Waele, E. Valgaeren, Joop Jonckheer, and K. Huysentruyt

Subjects
2019-20 coronavirus outbreak, medicine.medical_specialty, Nutrition and Dietetics, Coronavirus disease 2019 (COVID-19), business.industry, Endocrinology, Diabetes and Metabolism, Intensive care, Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), Emergency medicine, Energy metabolism, medicine, business, Article
Published
2021
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3. Iatrogenic malnutrition is more prevalent in critically ill covid-19 patients than in non-covid-19 patients, especially when discharged to the ward

Author

C. Verhelst, J. Geers, Joop Jonckheer, E. De Waele, J. Demol, and I. Loodts

Subjects
2019-20 coronavirus outbreak, medicine.medical_specialty, Nutrition and Dietetics, Coronavirus disease 2019 (COVID-19), business.industry, Critically ill, Endocrinology, Diabetes and Metabolism, Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), medicine.disease, Article, Malnutrition, Medicine, business, Intensive care medicine
Published
2021
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5. SYSTEMISCHE LUPUS ERYTHEMATOSUSGEASSOCIEERDE HEMOFAGOCYTAIRE LYMFOHISTIOCYTOSE

Author

A. Vonck, L.G.M.M. van Garsse, M. Dierick, F. Lacquet, and C. Verhelst

Subjects
Autoimmune disease, Gynecology, medicine.medical_specialty, Systemic disease, Lupus erythematosus, business.industry, Immunopathology, medicine, General Medicine, medicine.disease, business, Connective tissue disease
Abstract

Een patiente werd gehospitaliseerd met lymfadenopathie, koorts en een gegeneraliseeerd exantheem. Laboratoriumonderzoek toonde leucopenie, anemie, hyperferritinemie, verhoogde sedimentatie, gestegen CRP, complementverbruik, positieve anti-nuclaire factor-titer met positieve anti-dubbel strengig DNA antilichamen, negatieve p-ANCA en een fout positieve syfilis-test. Beenmergonderzoek toonde een groot aantal hemofagocyterende macrofagen. Diagnose van secundaire hemofagocytaire lymfohistiocytose bij een patiente met systemische lupus erythematosus werd vooropgesteld, een ernstige en soms fatale aandoening met vaak herhaalde opstoten van systemische lupus erythematosus, die langdurig actief kan blijven ondanks het gebruik van immunosuppressieve therapie. Hemofagocytaire lymfohistiocytose en systemische lupus erythematosus zijn vaak niet goed te onderscheiden, aangezien er frequent overlappingen zijn in klinische presentatie en biochemie. De diagnose berust op het klinisch beeld, bloed- en beenmergonder...

Published
2009
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6. Contents Vol. 121, 2009

Author

Eibhlin Conneally, Li An, Kanokwan Sanchaisuriya, A.S. Araújo, M.N.N. Santos, L.R.S. Vasconcelos, Nicholas C. Zoumbos, Hiroshi Handa, Yoshihisa Nojima, F. Lacquet, Eleni D. Lagadinou, A. Ruiz-Sáez, Maria K. Angelopoulou, Theodoros P. Vassilakopoulos, Maria Rosaria D'Apice, Yoshiaki Ishigatsubo, Arito Yamane, Shin Fujisawa, Giuseppa Penna, Hirotaka Nakahashi, Caterina Musolino, Hiroyuki Fujita, Naoto Tomita, M.M. Speeckaert, Jian Ouyang, P. Moura, Rie Hyo, Olga Tsopra, Jing Wang, Jun Taguchi, Kengo Takeuchi, Anila Mitre, Shigeki Motomura, Chizuko Hashimoto, Alessandro Allegra, C. Verhelst, Supan Fucharoen, Gyo Jun, A. Koch, Sarah Daly, Sachiya Takemura, Goonnapa Fucharoen, Argiris Symeonidis, M.S.M. Cavalcanti, Bing Chen, T.F. Mendonça, Thawalwong Ratanasiri, Hideki Uchiumi, Masaru Kojima, Jae-Won Park, Michela Biancolella, Gerassimos A. Pangalis, Nattaya Sae-ung, Hirokazu Murakami, Y. Tersek, Panos G. Ziros, Angela Granata, Andrea Alonci, Rossarin Karnpean, Giuseppe Novelli, Jeong-Soo Im, Yonggong Yang, R. Speeckaert, Leila Baghernajad-Salehi, Yun-Jae Jung, M.A.C. Bezerra, Patricia Rizzotti, Norifumi Tsukamoto, Ju Young Seoh, Koji Ogawa, Silvia Russo, Federica Sangiuolo, Masamitsu Karasawa, Arianna D'Angelo, R. Marchi Cappelletti, Eleni Thanopoulou, Takayuki Saitoh, Alexandra Kouraklis-Symeonidis, Stephen E. Langabeer, Shi Chen, Chang-Hoon Jeon, Nicola Di Daniele, Vahe Mokini, Anila Babameto-Laku, M.C.V.C. Oliveira, M. Meyer, and Rongfu Zhou

Subjects
Hematology, General Medicine
Published
2009
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7. A case of HELLP syndrome: an immuno-'logical' approach

Author

W A, Heggermont, C, Verhelst, K, De Wilde, M, De Paepe, F, Lacquet, and A, Vonck

Subjects
Adult, Blood Platelets, Diagnosis, Differential, HELLP Syndrome, Immunity, Cellular, Platelet Aggregation, Pregnancy, Pregnancy Outcome, Humans, Female, Follow-Up Studies
Abstract

We report on a 27-year-old woman who developed severe arterial hypertension on a background of general malaise within 48 hours after vaginal delivery, suggesting severe acute-onset pre-eclampsia. Concomitant biochemical observations of haemolysis, elevated liver tests and low platelets lead to the diagnosis of (post-partum) HELLP syndrome. Our patient was transferred immediately to the intensive care unit (ICU), where she underwent plasmapheresis in combination with intravenous glucocorticoids, nicardipine and labetalol. Our patient recovered fully after three plasmapheresis sessions. Genetic testing of mutations responsible for complement deficits was negative.

Published
2012

8. [Systemic lupus erythematosus over hemophagocytic lymphohistiocytosis]

Author

M, Dierick, F, Lacquet, C, Verhelst, A, Vonck, and L, Van Garsse

Subjects
Diagnosis, Differential, Killer Cells, Natural, Immunity, Cellular, Ferritins, Humans, Lupus Erythematosus, Systemic, Lymphohistiocytosis, Hemophagocytic
Abstract

A woman was admitted to the hospital with lymphadenopathy, fever and a generalised exanthema. Laboratory examination revealed leucopenia, anaemia, high sedimentation, elevated CRP and a markedly elevated serum ferritin. Further exploration showed a positive anti-nuclear factor-titre with anti-double-stranded DNA antibodies, positive p-ANCA and a falsely positive syphilis-test. Bone marrow examination revealed an elevated number of phagocytizing macrophages. Diagnosis of secondary haemophagocytic lymphohistiocytosis in a patient with systemic lupus erythematosus was made, a serious and sometimes fatal condition with often repeated exacerbations of the systemic lupus erythematosus that stays active for long periods in spite of the use of immunosuppressive therapy. Haemophagocytic lymphohistiocytosis and systemic lupus erythematosus are sometimes difficult to differentiate because the clinical presentation and laboratory findings are frequently very similar. The diagnosis depends on the clinical picture, blood and bone marrow examination. Bone marrow reveals an elevated haemophagocytosis. In patients with secondary haemophagocytic lymphohistiocytosis, the treatment of the underlying disorder is sometimes sufficient. In some cases there is need for a specific treatment with corticosteroids, intravenous immunoglobulin, immunosuppressive therapy or etoposide.

Published
2009

9. Subject Index Vol. 121, 2009

Author

Theodoros P. Vassilakopoulos, Nicola Di Daniele, Vahe Mokini, Bing Chen, A. Ruiz-Sáez, Maria K. Angelopoulou, Hirotaka Nakahashi, Yoshiaki Ishigatsubo, Jae-Won Park, Gerassimos A. Pangalis, Eibhlin Conneally, P. Moura, Anila Babameto-Laku, Hiroyuki Fujita, Maria Rosaria D'Apice, M.N.N. Santos, L.R.S. Vasconcelos, Anila Mitre, Jun Taguchi, Supan Fucharoen, Rie Hyo, Jing Wang, Gyo Jun, Yoshihisa Nojima, Shi Chen, A. Koch, Federica Sangiuolo, Alessandro Allegra, Masaru Kojima, Patricia Rizzotti, Rossarin Karnpean, Thawalwong Ratanasiri, Chang-Hoon Jeon, Nicholas C. Zoumbos, Hiroshi Handa, Silvia Russo, Andrea Alonci, Arianna D'Angelo, F. Lacquet, Eleni D. Lagadinou, Shin Fujisawa, R. Marchi Cappelletti, M.C.V.C. Oliveira, Eleni Thanopoulou, Norifumi Tsukamoto, M.A.C. Bezerra, Takayuki Saitoh, Ju Young Seoh, Kengo Takeuchi, M.M. Speeckaert, Li An, M.S.M. Cavalcanti, Alexandra Kouraklis-Symeonidis, Stephen E. Langabeer, Koji Ogawa, Leila Baghernajad-Salehi, T.F. Mendonça, Shigeki Motomura, Olga Tsopra, Yonggong Yang, C. Verhelst, Masamitsu Karasawa, Sachiya Takemura, Argiris Symeonidis, Sarah Daly, M. Meyer, Rongfu Zhou, R. Speeckaert, Jeong-Soo Im, Hirokazu Murakami, Y. Tersek, Angela Granata, Yun-Jae Jung, Michela Biancolella, Arito Yamane, Caterina Musolino, Naoto Tomita, A.S. Araújo, Hideki Uchiumi, Kanokwan Sanchaisuriya, Jian Ouyang, Chizuko Hashimoto, Giuseppa Penna, Nattaya Sae-ung, Goonnapa Fucharoen, Panos G. Ziros, and Giuseppe Novelli

Subjects
Index (economics), Statistics, Subject (documents), Hematology, General Medicine, Mathematics
Published
2009
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10. A case of HELLP syndrome: an immuno-"logical" approach.

Author

Heggermont WA, Verhelst C, De Wilde K, De Paepe M, Lacquet F, and Vonck A

Subjects
Adult, Diagnosis, Differential, Female, Follow-Up Studies, HELLP Syndrome immunology, HELLP Syndrome therapy, Humans, Pregnancy, Pregnancy Outcome, Blood Platelets immunology, HELLP Syndrome diagnosis, Immunity, Cellular, Platelet Aggregation immunology
Abstract

We report on a 27-year-old woman who developed severe arterial hypertension on a background of general malaise within 48 hours after vaginal delivery, suggesting severe acute-onset pre-eclampsia. Concomitant biochemical observations of haemolysis, elevated liver tests and low platelets lead to the diagnosis of (post-partum) HELLP syndrome. Our patient was transferred immediately to the intensive care unit (ICU), where she underwent plasmapheresis in combination with intravenous glucocorticoids, nicardipine and labetalol. Our patient recovered fully after three plasmapheresis sessions. Genetic testing of mutations responsible for complement deficits was negative.

Published
2012
Full Text
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11. Autoimmune haemolytic anaemia associated with a thymoma: case report and review of the literature.

Author

De Keyzer K, Peeters P, Verhelst C, Dendooven A, Vonck A, and Vanholder R

Subjects
Aged, Anemia, Hemolytic, Autoimmune drug therapy, Female, Glucocorticoids administration & dosage, Humans, Prednisone administration & dosage, Thymectomy, Thymoma pathology, Thymoma surgery, Thymus Neoplasms pathology, Thymus Neoplasms surgery, Anemia, Hemolytic, Autoimmune etiology, Thymoma complications, Thymus Neoplasms complications
Abstract

A 67-year-old female presents with a small mass in the anterior mediastinum on chest computed tomography. A biopsy proves the mass to be a spindle-cell-type or type A thymoma. Subsequently the patient develops fever and severe Coombs-positive haemolytic anaemia. She is initially treated with oral corticosteroids. Because of persistence of the haemolysis subsequent thymectomy is performed. Haemolysis disappears almost instantly and does not return after discontinuation of the oral corticosteroids. Review of the literature reveals only 17 other cases of thymoma-associated autoimmune haemolytic anaemia.

Published
2009
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12. [Systemic lupus erythematosus over hemophagocytic lymphohistiocytosis].

Author

Dierick M, Lacquet F, Verhelst C, Vonck A, and Van Garsse L

Subjects
Diagnosis, Differential, Ferritins blood, Humans, Killer Cells, Natural immunology, Killer Cells, Natural metabolism, Immunity, Cellular, Lupus Erythematosus, Systemic blood, Lupus Erythematosus, Systemic diagnosis, Lupus Erythematosus, Systemic immunology, Lymphohistiocytosis, Hemophagocytic blood, Lymphohistiocytosis, Hemophagocytic diagnosis, Lymphohistiocytosis, Hemophagocytic immunology
Abstract

A woman was admitted to the hospital with lymphadenopathy, fever and a generalised exanthema. Laboratory examination revealed leucopenia, anaemia, high sedimentation, elevated CRP and a markedly elevated serum ferritin. Further exploration showed a positive anti-nuclear factor-titre with anti-double-stranded DNA antibodies, positive p-ANCA and a falsely positive syphilis-test. Bone marrow examination revealed an elevated number of phagocytizing macrophages. Diagnosis of secondary haemophagocytic lymphohistiocytosis in a patient with systemic lupus erythematosus was made, a serious and sometimes fatal condition with often repeated exacerbations of the systemic lupus erythematosus that stays active for long periods in spite of the use of immunosuppressive therapy. Haemophagocytic lymphohistiocytosis and systemic lupus erythematosus are sometimes difficult to differentiate because the clinical presentation and laboratory findings are frequently very similar. The diagnosis depends on the clinical picture, blood and bone marrow examination. Bone marrow reveals an elevated haemophagocytosis. In patients with secondary haemophagocytic lymphohistiocytosis, the treatment of the underlying disorder is sometimes sufficient. In some cases there is need for a specific treatment with corticosteroids, intravenous immunoglobulin, immunosuppressive therapy or etoposide.

Published
2009
Full Text
View/download PDF

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