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29 results on '"De Angelis, Gioia"'

1. Nursing Management of Frail Patients with Hematologic Malignancies During COVID-19 Pandemia in the Viterbo Domiciliary Care Unit: Data Analysis from March 2020 to March 2021

Author

Ciambella, Silvia, primary, Innocenti, Vincenza, additional, Cippitelli, Elisa Emanueli, additional, Perazzino, Roberta, additional, Talucci, Roberta, additional, Panichi, Valentina, additional, Fiorini, Alessia, additional, Di Veroli, Ambra, additional, Mercanti, Caterina, additional, Natalino, Fiammetta, additional, De Angelis, Gioia, additional, Tarnani, Michela, additional, Morucci, Marco, additional, Mastini, Cristina, additional, Trapè, Giulio, additional, Silvestri, Assunta, additional, Montanaro, Marco, additional, and Latagliata, Roberto, additional

Published
2024
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2. The application of a multidisciplinary approach in the diagnosis of Castleman disease and Castleman‐like lymphadenopathies: A 20‐year retrospective analysis of clinical and pathological features

Author

Pelliccia, Sabrina, primary, Rogges, Evelina, additional, Cardoni, Antonello, additional, Lopez, Gianluca, additional, Conte, Esmeralda, additional, Faccini, Anna Laura, additional, De Vito, Rita, additional, Girardi, Katia, additional, Bianchi, Antonella, additional, Annibali, Ombretta, additional, Fratoni, Stefano, additional, Remotti, Daniele, additional, De Angelis, Gioia, additional, Giordano, Carla, additional, Palumbo, Giovanna, additional, Scarpino, Stefania, additional, Del Porto, Flavia, additional, Bianchi, Maria Paola, additional, Di Gregorio, Francesca, additional, Tafuri, Agostino, additional, and Di Napoli, Arianna, additional

Published
2023
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4. Pulmonary infections in patients with acute myeloid leukemia receiving frontline treatment with hypomethylating agents

Author

Scamuffa, Maria Cristina, primary, Latagliata, Roberto, additional, Carmosino, Ida, additional, Di Veroli, Ambra, additional, Scalzulli, Emilia, additional, Trapè, Giulio, additional, Ciotti, Giulia, additional, De Angelis, Gioia, additional, Tartaglia, Germana, additional, Tarnani, Michela, additional, Breccia, Massimo, additional, and Girmenia, Corrado, additional

Published
2023
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6. The application of a multidisciplinary approach in the diagnosis of Castleman disease and Castleman‐like lymphadenopathies: A 20‐year retrospective analysis of clinical and pathological features.

Author

Pelliccia, Sabrina, Rogges, Evelina, Cardoni, Antonello, Lopez, Gianluca, Conte, Esmeralda, Faccini, Anna Laura, De Vito, Rita, Girardi, Katia, Bianchi, Antonella, Annibali, Ombretta, Fratoni, Stefano, Remotti, Daniele, De Angelis, Gioia, Giordano, Carla, Palumbo, Giovanna, Scarpino, Stefania, Del Porto, Flavia, Bianchi, Maria Paola, Di Gregorio, Francesca, and Tafuri, Agostino

Subjects
LYMPHADENITIS, CASTLEMAN'S disease, DIAGNOSIS, MUCOSA-associated lymphoid tissue lymphoma, LYMPHOPROLIFERATIVE disorders, AUTOIMMUNE diseases
Abstract

Summary: Background: Castleman disease (CD) comprises a group of rare and heterogeneous haematological disorders, including unicentric (UCD) and multicentric (MCD) forms, the latter further subdivided into HHV8‐MCD, POEMS‐MCD and idiopathic‐MCD (iMCD). However, according to the Castleman Disease Collaborative Network guidelines, the diagnosis of CD can only be achieved through collaboration between clinicians and pathologists. Methods: We applied these clinical and pathological criteria and implement with clonality testing to a retrospective cohort of 48 adult and paediatric Italian patients diagnosed with reactive lymphadenitis with CD‐like histological features. Results: We confirmed the diagnosis of CD in 60% (29/48) of the cases, including 12 (41%) UCD and 17 (59%; five HHV8‐MCD, three POEMS‐MCD and nine iMCD) MCD. Of the remaining 19 cases (40%) with multiple lymphadenopathy, 5 (26%) were classified as autoimmune diseases, 1 (5%) as autoimmune lymphoproliferative disorder, 1 (5%) as IgG4‐related disease, 11 (83%) as reactive lymphadenitis and 1 (5%) as nodal marginal zone lymphoma. Conclusions: Our study emphasizes the importance of the multidisciplinary approach to reactive lymphadenitis with CD‐like features in order to achieve a definitive diagnosis and choose the appropriate treatment. [ABSTRACT FROM AUTHOR]

Published
2024
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8. Functional characterization and response to FLT3 inhibitors in acute myeloid leukaemia with a non‐canonical FLT3 mutation: A proof of concept

Author

Travaglini, Serena, primary, Gurnari, Carmelo, additional, Antonelli, Silvia, additional, Marchesi, Francesco, additional, De Angelis, Gioia, additional, Ottone, Tiziana, additional, Divona, Mariadomenica, additional, Cristiano, Antonio, additional, Hajrullaj, Hajro, additional, Mengarelli, Andrea, additional, and Voso, Maria Teresa, additional

Published
2023
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9. Treatment in patients with acute myeloid leukemia/high‐risk myelodysplastic syndrome with hypomethylating agents: Day‐hospital management compared to home care setting

Author

Trapè, Giulio, primary, De Angelis, Gioia, additional, Morucci, Marco, additional, Tarnani, Michela, additional, De Gregoris, Cinzia, additional, Di Veroli, Ambra, additional, Panichi, Valentina, additional, Topini, Giuseppe, additional, Bassi, Loredana, additional, Isidori, Raffaella, additional, Poscente, Monica, additional, Innocenti, Vincenza, additional, Cippitelli, Elisa Emanueli, additional, Talucci, Roberta, additional, Bertelli, Silvia, additional, Crocicchia, Alessandra, additional, Lippi, Annalisa, additional, Pezzuti, Giulia, additional, Fuschino, Michela, additional, Randi, Raffaella, additional, Mastini, Cristina, additional, Ciambella, Silvia, additional, Pessina, Gloria, additional, Montanaro, Marco, additional, and Latagliata, Roberto, additional

Published
2023
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10. Domiciliary Nursing Management for Patients Affected By Multiple Myeloma during Covid-19 Pandemia in the Viterbo Home Care Unit: Data Analysis from March 2020 to March 2022

Author

Emanueli Cippitelli, Elisa, primary, Innocenti, Vincenza, additional, De Angelis, Gioia, additional, Bertelli, Silvia, additional, Talucci, Roberta, additional, Perazzini, Roberta, additional, Burla, Roberta, additional, Panichi, Valentina, additional, Topini, Giuseppe, additional, Di Veroli, Ambra, additional, Fiorini, Alessia, additional, Mercanti, Caterina, additional, Natalino, Fiammetta, additional, Stefanizzi, Caterina, additional, De Gregoris, Cinzia, additional, Tarnani, Michela, additional, Morucci, Marco, additional, Mastino, Cristina, additional, Trapè, Giulio, additional, Montanaro, Marco, additional, Latagliata, Roberto, additional, and Ciambella, Silvia, additional

Published
2022
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11. Structural and Functional Insights on an Uncharacterized Aγ-Globin-Gene Polymorphism Present in Four β0-Thalassemia Families with High Fetal Hemoglobin Levels

Author

Bianchi, Nicoletta, Cosenza, Lucia Carmela, Lampronti, Ilaria, Finotti, Alessia, Breveglieri, Giulia, Zuccato, Cristina, Fabbri, Enrica, Marzaro, Giovanni, Chilin, Adriana, De Angelis, Gioia, Borgatti, Monica, Gallucci, Cristiano, Alfieri, Cecilia, Ribersani, Michela, Isgrò, Antonella, Marziali, Marco, Gaziev, Javid, Morrone, Aldo, Sodani, Pietro, Lucarelli, Guido, Gambari, Roberto, and Paciaroni, Katia

Published
2016
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12. Nursing Management of Frail Patients with Hematologic Malignancies during COVID-19 Pandemia in the Viterbo Domiciliary Care Unit: Data Analysis from March 2020 to March 2021

Author

Ciambella, Silvia, primary, Innocenti, Vincenza, additional, Emanueli Cippitelli, Elisa, additional, Bertelli, Silvia, additional, Talucci, Roberta, additional, Panichi, Valentina, additional, Topini, Giuseppe, additional, Fiorini, Alessia, additional, Di Veroli, Ambra, additional, Mercanti, Caterina, additional, Natalino, Fiammetta, additional, De Angelis, Gioia, additional, Tarnani, Michela, additional, Morucci, Marco, additional, Mastino, Cristina, additional, Stagno, Fabio, additional, Trapè, Giulio, additional, Silvestri, Assunta, additional, Montanaro, Marco, additional, and Latagliata, Roberto, additional

Published
2021
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13. Azacytidine Treatment in Patients with Acute Myeloid Leukemia/High-Risk Myelodysplastic Syndrome: Day-Hospital Management Compared to Home Care Setting

Author

Trapè, Giulio, primary, De Angelis, Gioia, additional, Morucci, Marco, additional, Tarnani, Michela, additional, De Gregoris, Cinzia, additional, Di Veroli, Ambra, additional, Panichi, Valentina, additional, Topini, Giuseppe, additional, Bassi, Loredana, additional, Isidori, Raffaella, additional, Poscente, Monica, additional, Innocenti, Vincenza, additional, Emanueli Cippitelli, Elisa, additional, Talucci, Roberta, additional, Bertelli, Silvia, additional, Crocicchia, Alessandra, additional, Lippi, Annalisa, additional, Pezzuti, Giulia, additional, Fuschino, Michela, additional, Randi, Raffaella, additional, Mastino, Cristina, additional, Ciambella, Silvia, additional, Pessina, Gloria, additional, Montanaro, Marco, additional, and Latagliata, Roberto, additional

Published
2021
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14. New insights into the pharmacokinetics of intravenous busulfan in children with sickle cell anemia undergoing bone marrow transplantation

Author

Gaziev, Javid, Isgrò, Antonella, Mozzi, Alessia Francesca, Petain, Aurèlie, Nguyen, Laurent, Ialongo, Cristiano, Dinallo, Vincenzo, Sodani, Pietro, Marziali, Marco, Andreani, Marco, Testi, Manuela, Paciaroni, Katia, Gallucci, Cristiano, De Angelis, Gioia, Alfieri, Cecilia, Ribersani, Michela, and Lucarelli, Guido

Published
2015
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15. Subcutaneous Daratumumab at Home Is a Safe and Effective Procedure for Frail Patients with Multiple Myeloma: A Myelhome Project Report

Author

De Angelis, Gioia, Fiorini, Alessia, Trapè, Giulio, Panichi, Valentina, Chavez, Maria Gabriela, Emanueli Cippitelli, Elisa, Innocenti, Vincenza, Perazzini, Roberta, Talucci, Roberta, Topini, Giuseppe, Di Veroli, Ambra, Mercanti, Caterina, Natalino, Fiammetta, Tarnani, Michela, Morucci, Marco, Mastini, Cristina, Silvestri, Assunta, Andriani, Alessandro, Montanaro, Marco, Ciambella, Silvia, and Latagliata, Roberto

Published
2023
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19. Long-Term Outcome after Haploidentical Hematopoietic Cell Transplantation Utilizing CD34+ Selected/CD3CD19+ Depleted or Tcrαβ+/CD19+ Depleted Grafts in Pediatric Patients with Hemoglobinopathies

Author

Gaziev, Javid, primary, Isgrò, Antonella, additional, Sodani, Pietro, additional, Paciaroni, Katia, additional, De Angelis, Gioia, additional, Marziali, Marco, additional, Ribersani, Michela, additional, Alfieri, Cecilia, additional, Andreani, Marco, additional, Gallucci, Tiziana, additional, and Lucarelli, Guido, additional

Published
2017
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23. Optimal Outcomes in Young Class 3 Patients With Thalassemia Undergoing HLA-Identical Sibling Bone Marrow Transplantation

Author

Gaziev, Javid, primary, Isgrò, Antonella, additional, Sodani, Pietro, additional, Marziali, Marco, additional, Paciaroni, Katia, additional, Gallucci, Cristiano, additional, De Angelis, Gioia, additional, Andreani, Marco, additional, Testi, Manuela, additional, Alfieri, Cecilia, additional, Ribersani, Michela, additional, Galluccio, Tiziana, additional, Battarra, Maria Rosa, additional, Morrone, Aldo, additional, and Lucarelli, Guido, additional

Published
2016
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24. Transplant Outcomes in High-Risk (Class 3) Patients with Thalassemia Treated with a Modified Protocol Are Equivalent to Low/Intermediate-Risk (Class 1/Class 2) Patients

Author

Gaziev, Javid, primary, De Angelis, Gioia, additional, Isgro, Antonella, additional, Sodani, Pietro, additional, Marziali, Marco, additional, Paciaroni, Katia, additional, Andreani, Marco, additional, Testi, Manuela, additional, Gallucci, Cristiano, additional, Alfieri, Cecilia, additional, Ribersani, Michela, additional, Troiano, Maria, additional, Morrone, Aldo, additional, and Lucarelli, Guido, additional

Published
2015
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25. Hematopoietic Stem Cell Transplantation in Nigerian Children with Sickle Cell Anemia

Author

Isgro, Antonella, primary, Gaziev, Javid, additional, Sodani, Pietro, additional, Andreani, Marco, additional, Testi, Manuela, additional, Paciaroni, Katia, additional, Gallucci, Cristiano, additional, De Angelis, Gioia, additional, Marziali, Marco, additional, Alfieri, Cecilia, additional, Ribersani, Michela, additional, Akinyanju, Olufemi O, additional, Wakama, T. Thompson, additional, Olowoselu, Festus Olusola, additional, and Lucarelli, Guido, additional

Published
2015
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26. Invasive Pulmonary Aspergillosis in a Sickle Cell Patient Transplant Recipient: A Successful Treatment

Author

Paciaroni, Katia, primary, De Angelis, Gioia, primary, Gallucci, Cristiano, primary, Alfieri, Cecilia, primary, Ribersani, Michela, primary, Roveda, Andrea, primary, Isgrò, Antonella, primary, Marziali, Marco, primary, Aloi, Ivan Pietro, primary, Inserra, Alessandro, primary, Gaziev, Javid, primary, Sodani, Pietro, primary, and Lucarelli, Guido, primary

Published
2015
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27. Haematopoietic stem cell transplantation in Nigerian sickle cell anaemia children patients.

Author

Isgrò, Antonella, Paciaroni, Katia, Gaziev, Javid, Sodani, Pietro, Gallucci, Cristiano, Marziali, Marco, De Angelis, Gioia, Alfieri, Cecilia, Ribersani, Michela, Roveda, Andrea, Akinyanju, Olufemi O., Thompson Wakama, T., Olowoselu, Festus Olusola, Adediran, Adewumi, and Lucarelli, Guido

Subjects
HAEMATOPODIDAE, STEM cell transplantation, SICKLE cell anemia, BONE marrow transplantation, MYELOSUPPRESSION
Abstract

Background: Sickle cell anaemia (SCA) remains associated with high risks of morbidity and early death. Children with SCA are at high risk for ischaemic stroke and transient ischaemic attacks, secondary to intracranial arteriopathy involving carotid and cerebral arteries. Allogeneic haematopoietic stem cell transplantation (HSCT) is the only curative treatment for SCA. We report our experience with transplantation in a group of patients with the Black African variant of SCA. Patients and Methods: This study included 31 consecutive SCA patients who underwent bone marrow transplantation from human leukocyte antigen (HLA)-identical sibling donors between 2010 and 2014 following a myeloablative-conditioning regimen. Results: The median patient age was 10 years (range 2-17 years). Before transplantation, 14 patients had recurrent, painful, vaso-occlusive crisis; ten patients had recurrent painful crisis in association with acute chest syndrome; three patients experienced ischaemic stroke and recurrent vaso-occlusive crisis; two patients experienced ischaemic stroke; one patient exhibited leukocytosis; and one patient exhibited priapism. Of the 31 patients, 28 survived without sickle cell disease, with Lansky/Karnofsky scores of 100. All surviving patients remained free of any SCA-related events after transplantation. Conclusion: The protocols used for the preparation to the transplant in thalassaemia are very effective also in the other severe haemoglobinopathy as in the sickle cell anaemia with 90% disease free survival. Today, if a SCA patient has a HLA identical family member, the cellular gene therapy through the transplantation of the allogeneic haemopoietic cell should be performed. Tomorrow, hopefully, the autologous genetically corrected stem cell will break down the wall of the immunological incompatibility. [ABSTRACT FROM AUTHOR]

Published
2015
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29. Invasive pulmonary aspergillosis in a haematopoietic stem cell transplant recipient with sickle cell disease: a successful treatment.

Author

Paciaroni K, De Angelis G, Gallucci C, Alfieri C, Ribersani M, Roveda A, Isgrò A, Marziali M, Aloi IP, Inserra A, Gaziev J, Sodani P, and Lucarelli G

Abstract

Sickle Cell Anaemia (SCA) is the most common inherited blood disorder and is associated with severe morbidity and decreased survival. Allogeneic Haematopoietic Stem Cell Transplantation (HSCT) is the only curative approach. Nevertheless the decision to perform a bone marrow transplant includes the risk of major complications and transplant-related mortality. Infections represent the leading cause of death in SCA patients undergoing HSCT. Invasive Pulmonary Aspergillosis (IPA) is a devastating opportunistic infection and remains a significant cause of morbidity and mortality in HSCT recipients. Data regarding IPA in the setting of SCA are lacking. In the present report, we describe a patient with SCA, who developed IPA after allogeneic bone marrow transplant. The fungal infection was treated by systemic antifungal therapy in addition to surgery, despite mild chronic graft versus host disease (GVHD) and continuing immunosuppressive therapy. This case shows that IPA occurring in bone marrow recipients with SCA can be successfully treated.

Published
2015
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