Haemophilic Pelvic Pseudotumour: A New Surgical Option

Background: Haemophilia is an inherited coagulopathy caused by the absence or dysfunction of clotting factor VIII or IX. Clinical manifestations are generally secondary to recurrent bleeding episodes mainly in the musculoskeletal system. Bleeding symptoms appear early in life and, when the disease i...
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Autor*in:	Gianluigi Pasta [verfasserIn] Roberta Ruggieri [verfasserIn] Salvatore Annunziata [verfasserIn] Alessandro Gallese [verfasserIn] Vincenzo Pio Gagliardi [verfasserIn] Fabrizio Cuzzocrea [verfasserIn] Matteo Ghiara [verfasserIn] Mariaconcetta Russo [verfasserIn] Paola Stefania Preti [verfasserIn] Roberto Mario Santi [verfasserIn] Mario Mosconi [verfasserIn] Francesco Benazzo [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2021

Schlagwörter:	haemophilia pseudotumour pelvis perioperative management surgical treatment complication

Übergeordnetes Werk:	In: Healthcare - MDPI AG, 2013, 9(2021), 10, p 1269
Übergeordnetes Werk:	volume:9 ; year:2021 ; number:10, p 1269

Links:	Link aufrufen Link aufrufen Link aufrufen Journal toc

DOI / URN:	10.3390/healthcare9101269

Katalog-ID:	DOAJ051538024

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allfields	10.3390/healthcare9101269 doi (DE-627)DOAJ051538024 (DE-599)DOAJ219ccf7734e14a83b2d16c6f298e52b9 DE-627 ger DE-627 rakwb eng Gianluigi Pasta verfasserin aut Haemophilic Pelvic Pseudotumour: A New Surgical Option 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Background: Haemophilia is an inherited coagulopathy caused by the absence or dysfunction of clotting factor VIII or IX. Clinical manifestations are generally secondary to recurrent bleeding episodes mainly in the musculoskeletal system. Bleeding symptoms appear early in life and, when the disease is severe (when plasma factor VIII or IX activity is <1% of normal), joint and muscle bleeding may occur spontaneously. A pseudotumour is a recurrent, chronic, encapsulated, slowly expanding, muscle hematoma. Haemophilic pseudotumour is a rare complication of haemophilia which occurs, as a condition either from repeated spontaneous bleeding or coming from a traumatic origin, in 1–2% of haemophilic patients. Case report: A 32-year-old man with severe haemophilia A referred to our Clinic with a massive right iliac wing pseudotumour complicated by Staphylococcus aureus superinfection and skin fistulisation. In this report we describe the medical management and surgical treatment by the adoption of a novel surgical technique which involves the use of a pedicle-screw and rod system (PSRS), a polyglycolic acid MESH and bone cement in order to build up an artificial ilium-like bony mass. This case report highlights the importance of interdisciplinary approach and the efficacy of eradicating surgery as treatment, especially in the case of large and long-lasting lesions. haemophilia pseudotumour pelvis perioperative management surgical treatment complication Medicine R Roberta Ruggieri verfasserin aut Salvatore Annunziata verfasserin aut Alessandro Gallese verfasserin aut Vincenzo Pio Gagliardi verfasserin aut Fabrizio Cuzzocrea verfasserin aut Matteo Ghiara verfasserin aut Mariaconcetta Russo verfasserin aut Paola Stefania Preti verfasserin aut Roberto Mario Santi verfasserin aut Mario Mosconi verfasserin aut Francesco Benazzo verfasserin aut In Healthcare MDPI AG, 2013 9(2021), 10, p 1269 (DE-627)750371544 (DE-600)2721009-1 22279032 nnns volume:9 year:2021 number:10, p 1269 https://doi.org/10.3390/healthcare9101269 kostenfrei https://doaj.org/article/219ccf7734e14a83b2d16c6f298e52b9 kostenfrei https://www.mdpi.com/2227-9032/9/10/1269 kostenfrei https://doaj.org/toc/2227-9032 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 9 2021 10, p 1269
spelling	10.3390/healthcare9101269 doi (DE-627)DOAJ051538024 (DE-599)DOAJ219ccf7734e14a83b2d16c6f298e52b9 DE-627 ger DE-627 rakwb eng Gianluigi Pasta verfasserin aut Haemophilic Pelvic Pseudotumour: A New Surgical Option 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Background: Haemophilia is an inherited coagulopathy caused by the absence or dysfunction of clotting factor VIII or IX. Clinical manifestations are generally secondary to recurrent bleeding episodes mainly in the musculoskeletal system. Bleeding symptoms appear early in life and, when the disease is severe (when plasma factor VIII or IX activity is <1% of normal), joint and muscle bleeding may occur spontaneously. A pseudotumour is a recurrent, chronic, encapsulated, slowly expanding, muscle hematoma. Haemophilic pseudotumour is a rare complication of haemophilia which occurs, as a condition either from repeated spontaneous bleeding or coming from a traumatic origin, in 1–2% of haemophilic patients. Case report: A 32-year-old man with severe haemophilia A referred to our Clinic with a massive right iliac wing pseudotumour complicated by Staphylococcus aureus superinfection and skin fistulisation. In this report we describe the medical management and surgical treatment by the adoption of a novel surgical technique which involves the use of a pedicle-screw and rod system (PSRS), a polyglycolic acid MESH and bone cement in order to build up an artificial ilium-like bony mass. This case report highlights the importance of interdisciplinary approach and the efficacy of eradicating surgery as treatment, especially in the case of large and long-lasting lesions. haemophilia pseudotumour pelvis perioperative management surgical treatment complication Medicine R Roberta Ruggieri verfasserin aut Salvatore Annunziata verfasserin aut Alessandro Gallese verfasserin aut Vincenzo Pio Gagliardi verfasserin aut Fabrizio Cuzzocrea verfasserin aut Matteo Ghiara verfasserin aut Mariaconcetta Russo verfasserin aut Paola Stefania Preti verfasserin aut Roberto Mario Santi verfasserin aut Mario Mosconi verfasserin aut Francesco Benazzo verfasserin aut In Healthcare MDPI AG, 2013 9(2021), 10, p 1269 (DE-627)750371544 (DE-600)2721009-1 22279032 nnns volume:9 year:2021 number:10, p 1269 https://doi.org/10.3390/healthcare9101269 kostenfrei https://doaj.org/article/219ccf7734e14a83b2d16c6f298e52b9 kostenfrei https://www.mdpi.com/2227-9032/9/10/1269 kostenfrei https://doaj.org/toc/2227-9032 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 9 2021 10, p 1269
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allfieldsSound	10.3390/healthcare9101269 doi (DE-627)DOAJ051538024 (DE-599)DOAJ219ccf7734e14a83b2d16c6f298e52b9 DE-627 ger DE-627 rakwb eng Gianluigi Pasta verfasserin aut Haemophilic Pelvic Pseudotumour: A New Surgical Option 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Background: Haemophilia is an inherited coagulopathy caused by the absence or dysfunction of clotting factor VIII or IX. Clinical manifestations are generally secondary to recurrent bleeding episodes mainly in the musculoskeletal system. Bleeding symptoms appear early in life and, when the disease is severe (when plasma factor VIII or IX activity is <1% of normal), joint and muscle bleeding may occur spontaneously. A pseudotumour is a recurrent, chronic, encapsulated, slowly expanding, muscle hematoma. Haemophilic pseudotumour is a rare complication of haemophilia which occurs, as a condition either from repeated spontaneous bleeding or coming from a traumatic origin, in 1–2% of haemophilic patients. Case report: A 32-year-old man with severe haemophilia A referred to our Clinic with a massive right iliac wing pseudotumour complicated by Staphylococcus aureus superinfection and skin fistulisation. In this report we describe the medical management and surgical treatment by the adoption of a novel surgical technique which involves the use of a pedicle-screw and rod system (PSRS), a polyglycolic acid MESH and bone cement in order to build up an artificial ilium-like bony mass. This case report highlights the importance of interdisciplinary approach and the efficacy of eradicating surgery as treatment, especially in the case of large and long-lasting lesions. haemophilia pseudotumour pelvis perioperative management surgical treatment complication Medicine R Roberta Ruggieri verfasserin aut Salvatore Annunziata verfasserin aut Alessandro Gallese verfasserin aut Vincenzo Pio Gagliardi verfasserin aut Fabrizio Cuzzocrea verfasserin aut Matteo Ghiara verfasserin aut Mariaconcetta Russo verfasserin aut Paola Stefania Preti verfasserin aut Roberto Mario Santi verfasserin aut Mario Mosconi verfasserin aut Francesco Benazzo verfasserin aut In Healthcare MDPI AG, 2013 9(2021), 10, p 1269 (DE-627)750371544 (DE-600)2721009-1 22279032 nnns volume:9 year:2021 number:10, p 1269 https://doi.org/10.3390/healthcare9101269 kostenfrei https://doaj.org/article/219ccf7734e14a83b2d16c6f298e52b9 kostenfrei https://www.mdpi.com/2227-9032/9/10/1269 kostenfrei https://doaj.org/toc/2227-9032 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 9 2021 10, p 1269
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author	Gianluigi Pasta
spellingShingle	Gianluigi Pasta misc haemophilia misc pseudotumour misc pelvis misc perioperative management misc surgical treatment misc complication misc Medicine misc R Haemophilic Pelvic Pseudotumour: A New Surgical Option
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topic_title	Haemophilic Pelvic Pseudotumour: A New Surgical Option haemophilia pseudotumour pelvis perioperative management surgical treatment complication
topic	misc haemophilia misc pseudotumour misc pelvis misc perioperative management misc surgical treatment misc complication misc Medicine misc R
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title	Haemophilic Pelvic Pseudotumour: A New Surgical Option
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title_full	Haemophilic Pelvic Pseudotumour: A New Surgical Option
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author_browse	Gianluigi Pasta Roberta Ruggieri Salvatore Annunziata Alessandro Gallese Vincenzo Pio Gagliardi Fabrizio Cuzzocrea Matteo Ghiara Mariaconcetta Russo Paola Stefania Preti Roberto Mario Santi Mario Mosconi Francesco Benazzo
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title_sort	haemophilic pelvic pseudotumour: a new surgical option
title_auth	Haemophilic Pelvic Pseudotumour: A New Surgical Option
abstract	Background: Haemophilia is an inherited coagulopathy caused by the absence or dysfunction of clotting factor VIII or IX. Clinical manifestations are generally secondary to recurrent bleeding episodes mainly in the musculoskeletal system. Bleeding symptoms appear early in life and, when the disease is severe (when plasma factor VIII or IX activity is <1% of normal), joint and muscle bleeding may occur spontaneously. A pseudotumour is a recurrent, chronic, encapsulated, slowly expanding, muscle hematoma. Haemophilic pseudotumour is a rare complication of haemophilia which occurs, as a condition either from repeated spontaneous bleeding or coming from a traumatic origin, in 1–2% of haemophilic patients. Case report: A 32-year-old man with severe haemophilia A referred to our Clinic with a massive right iliac wing pseudotumour complicated by Staphylococcus aureus superinfection and skin fistulisation. In this report we describe the medical management and surgical treatment by the adoption of a novel surgical technique which involves the use of a pedicle-screw and rod system (PSRS), a polyglycolic acid MESH and bone cement in order to build up an artificial ilium-like bony mass. This case report highlights the importance of interdisciplinary approach and the efficacy of eradicating surgery as treatment, especially in the case of large and long-lasting lesions.
abstractGer	Background: Haemophilia is an inherited coagulopathy caused by the absence or dysfunction of clotting factor VIII or IX. Clinical manifestations are generally secondary to recurrent bleeding episodes mainly in the musculoskeletal system. Bleeding symptoms appear early in life and, when the disease is severe (when plasma factor VIII or IX activity is <1% of normal), joint and muscle bleeding may occur spontaneously. A pseudotumour is a recurrent, chronic, encapsulated, slowly expanding, muscle hematoma. Haemophilic pseudotumour is a rare complication of haemophilia which occurs, as a condition either from repeated spontaneous bleeding or coming from a traumatic origin, in 1–2% of haemophilic patients. Case report: A 32-year-old man with severe haemophilia A referred to our Clinic with a massive right iliac wing pseudotumour complicated by Staphylococcus aureus superinfection and skin fistulisation. In this report we describe the medical management and surgical treatment by the adoption of a novel surgical technique which involves the use of a pedicle-screw and rod system (PSRS), a polyglycolic acid MESH and bone cement in order to build up an artificial ilium-like bony mass. This case report highlights the importance of interdisciplinary approach and the efficacy of eradicating surgery as treatment, especially in the case of large and long-lasting lesions.
abstract_unstemmed	Background: Haemophilia is an inherited coagulopathy caused by the absence or dysfunction of clotting factor VIII or IX. Clinical manifestations are generally secondary to recurrent bleeding episodes mainly in the musculoskeletal system. Bleeding symptoms appear early in life and, when the disease is severe (when plasma factor VIII or IX activity is <1% of normal), joint and muscle bleeding may occur spontaneously. A pseudotumour is a recurrent, chronic, encapsulated, slowly expanding, muscle hematoma. Haemophilic pseudotumour is a rare complication of haemophilia which occurs, as a condition either from repeated spontaneous bleeding or coming from a traumatic origin, in 1–2% of haemophilic patients. Case report: A 32-year-old man with severe haemophilia A referred to our Clinic with a massive right iliac wing pseudotumour complicated by Staphylococcus aureus superinfection and skin fistulisation. In this report we describe the medical management and surgical treatment by the adoption of a novel surgical technique which involves the use of a pedicle-screw and rod system (PSRS), a polyglycolic acid MESH and bone cement in order to build up an artificial ilium-like bony mass. This case report highlights the importance of interdisciplinary approach and the efficacy of eradicating surgery as treatment, especially in the case of large and long-lasting lesions.
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title_short	Haemophilic Pelvic Pseudotumour: A New Surgical Option
url	https://doi.org/10.3390/healthcare9101269 https://doaj.org/article/219ccf7734e14a83b2d16c6f298e52b9 https://www.mdpi.com/2227-9032/9/10/1269 https://doaj.org/toc/2227-9032
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author2	Roberta Ruggieri Salvatore Annunziata Alessandro Gallese Vincenzo Pio Gagliardi Fabrizio Cuzzocrea Matteo Ghiara Mariaconcetta Russo Paola Stefania Preti Roberto Mario Santi Mario Mosconi Francesco Benazzo
author2Str	Roberta Ruggieri Salvatore Annunziata Alessandro Gallese Vincenzo Pio Gagliardi Fabrizio Cuzzocrea Matteo Ghiara Mariaconcetta Russo Paola Stefania Preti Roberto Mario Santi Mario Mosconi Francesco Benazzo
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up_date	2024-07-03T20:56:10.596Z
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Haemophilic Pelvic Pseudotumour: A New Surgical Option

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