Les complications incluent la métastase, la douleur chronique et des problèmes fonctionnels.
ComplicationsLéiomyosarcomeMétastase
#2
Le léiomyosarcome peut-il se propager ?
Oui, il peut se propager à d'autres organes, notamment les poumons et le foie.
MétastaseLéiomyosarcomePropagation
#3
Y a-t-il des risques liés aux traitements ?
Oui, les traitements peuvent entraîner des effets secondaires comme la fatigue et des nausées.
Effets secondairesLéiomyosarcomeTraitements
#4
Comment gérer la douleur liée au léiomyosarcome ?
La gestion de la douleur peut inclure des médicaments, la physiothérapie et des soins palliatifs.
Gestion de la douleurLéiomyosarcomeSoins palliatifs
#5
Le suivi post-traitement est-il crucial ?
Oui, un suivi régulier est essentiel pour surveiller les récidives et gérer les complications.
Suivi post-traitementLéiomyosarcomeRécidive
Facteurs de risque
5
#1
Quels sont les principaux facteurs de risque ?
Les facteurs incluent l'exposition à des radiations, des produits chimiques et des antécédents familiaux.
Facteurs de risqueLéiomyosarcomeRadiations
#2
L'âge influence-t-il le risque de léiomyosarcome ?
Oui, le risque augmente généralement avec l'âge, touchant souvent les adultes d'âge moyen.
ÂgeLéiomyosarcomeRisque
#3
Les maladies génétiques sont-elles un facteur ?
Certaines maladies génétiques, comme le syndrome de Li-Fraumeni, augmentent le risque.
Maladies génétiquesLéiomyosarcomeSyndrome de Li-Fraumeni
#4
Le sexe joue-t-il un rôle dans le risque ?
Oui, les femmes sont légèrement plus susceptibles de développer un léiomyosarcome utérin.
SexeLéiomyosarcomeRisque
#5
L'obésité est-elle un facteur de risque ?
Oui, l'obésité peut être associée à un risque accru de certains types de sarcomes, y compris le léiomyosarcome.
ObésitéLéiomyosarcomeRisque
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"acceptedAnswer": {
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"@type": "Question",
"name": "La chirurgie est-elle toujours nécessaire ?",
"position": 17,
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{
"@type": "Question",
"name": "La chimiothérapie est-elle efficace ?",
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"position": 19,
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"name": "Y a-t-il des traitements expérimentaux ?",
"position": 20,
"acceptedAnswer": {
"@type": "Answer",
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}
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"@type": "Question",
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"@type": "Question",
"name": "Les maladies génétiques sont-elles un facteur ?",
"position": 28,
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"@type": "Question",
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Splenectomy is performed in 4-32% of cytoreductive surgeries for ovarian cancer. The objective of our study was to assess splenectomy and evaluate its impact on overall and disease-free survival....
We conducted a retrospective single-center study between January 2000 and December 2016. Patients who underwent a cytoreduction for epithelial ovarian cancer, regardless of stage and surgical approach...
This cohort included 464 patients. Disease stages, peritoneal carcinomatosis scores, and the rate of radical surgery (Pomel classification) were significantly higher in the splenectomy group, p=0.04, ...
Splenectomy may be considered an acceptable and safe procedure; however, with no impact on overall or disease-free survival. In addition, it is associated with longer hospital stay and longer time to ...
Splenectomy impacts hematological, immunological, and metabolic functions of the patient. Since our understanding of its metabolic effects, in particular effects on lipid metabolism, is limited, this ...
The data from 316 patients undergoing splenectomy between 2009 and 2019 were retrospectively analyzed. Thirty-eight patients whose serum lipid values were measured both preoperatively and 1 year after...
Significantly higher levels of total cholesterol, low-density lipoprotein (LDL), and non-high-density lipoprotein (HDL) lipid profile were found in the postsplenectomy measurements. However, no signif...
We determined that splenectomy does impact lipid metabolism, and that the metabolic effects of splenectomy should further be investigated....
Whether COVID-19-related morbidity and mortality are increased in splenectomized patients is unknown. The study by Bianchi et al. suggests increased hospitalizations and mortality rates in splenectomi...
Hemophagocytic syndrome or hemophagocytic lymphohistiocytosis (HL) is an immune hyperactivation of multifactorial etiology, characterized by excessive activation of lymphocytes and macrophages, as wel...
38-year-old male patient without comorbidities, who presented with abdominal pain, choluria, fever > 38 °C and diaphoresis of more than 10 days of evolution. A bone marrow aspirate was performed as pa...
Splenectomy increases the overall survival rate and the time free of HL progression, even though there are still no studies to determine with certainty the ideal time to perform a splenectomy in patie...
Splenic B-cell lymphomas are rare and understudied entities. Splenectomy is frequently required for specific pathological diagnosis in patients with splenic B-cell lymphomas other than classical hairy...
Observational study of patients with non-cHCL splenic B-cell lymphoma undergoing splenectomy between 1 August 2011 and 1 August 2021 at the University of Rochester Medical Center. The comparison cohor...
Forty-nine patients (median age 68 years) had splenectomy (SMZL n = 33, HCLv n = 9, SDRPL n = 7) with median follow up of 3.9 years post splenectomy. One patient had fatal post-operative complications...
Splenectomy is useful for the diagnosis of non-cHCL splenic B-cell lymphomas with comparable risk/benefit profile and remission duration to medical therapy. Patients with suspected non-cHCL splenic ly...
Takenouchi-Kosaki syndrome (TKS) is a rare congenital disease caused by a de novo heterozygous mutation in the CDC42 gene. Its characteristic clinical features are macrothrombocytopenia, developmental...
Gallstones are common in hereditary spherocytosis (HS) and other chronic hemolytic diseases, with most affected patients being asymptomatic. Whether and how asymptomatic gallstones should be treated i...
We conducted a retrospective cohort study of pediatric patients with HS and asymptomatic gallstones to compare the clinical outcomes between the observation group (followed up with gallstones in situ)...
Fifty-two patients were included (38 in the observation group and 14 in the intervention group), with a mean follow-up length of 5.2 years. Patients in the intervention group had a lower incidence of ...
Most asymptomatic gallstones grow or persist in splenectomized HS patients for an extended period. Surgical treatment of asymptomatic gallstones in HS patients requiring splenectomy is associated with...
III (retrospective comparative study)....
The infectious burden in hereditary spherocytosis (HS) children before splenectomy has rarely been reported and the risk of severe postsplenectomy infection is controversial....
We conducted a retrospective study of pediatric patients with HS to evaluate the risk of infection presplenectomy and postsplenectomy. The primary outcome was any bacterial, Mycoplasma, or fungal infe...
In all, 232 patients were included. Before splenectomy, the primary outcome was identified in 51 (22.0%) patients, and the secondary outcome was identified in 1 (0.4%) patient. After splenectomy, the ...
HS patients who require splenectomy later in life had a high incidence of hospitalization for infections. In contrast, postsplenectomy risk of hospitalization involving infection or severe infection w...
Patients with hereditary spherocytosis who require splenectomy later in life have a high risk of hospital admission for infections, especially those with severe hereditary spherocytosis. With vaccines...
Since its introduction in 1991, laparoscopic splenectomy has been considered the gold standard in spleen surgery, and the advantages of this technique over open surgery are indisputable. The technique...
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked genetic disease caused by a pathogenic G6PD mutation. An 8-year-old Chinese male child was investigated because of chronic nonspheroc...