Assuntos
Anemia Hemolítica Autoimune/complicações , Eritrócitos/patologia , Transtornos Leucocíticos/patologia , Fagocitose , Trombocitose/complicações , Idoso de 80 Anos ou mais , Anemia Hemolítica Autoimune/terapia , Humanos , Transtornos Leucocíticos/sangue , Transtornos Leucocíticos/etiologia , Masculino , Trombocitose/terapiaRESUMO
We present the case of an HIV-negative man in his 50s who developed a generalised nodular rash while having first-line bortezomib-cyclophosphamide-dexamethasone chemotherapy for multiple myeloma. The rash was biopsied and proven to be Kaposi's sarcoma. The patient's treatment was interrupted at the sixth cycle of chemotherapy, by which time the rash had also spread to the oral mucosa and eyelid. The rash regressed spontaneously on stopping treatment. We were reluctant to restart myeloma treatment, but on the other hand, we wished to consolidate the very good partial response achieved. An autologous marrow transplant was done months later without any recurrence of his Kaposi's with the initiation of bortezomib maintenance. Bortezomib has putative activity against Kaposi's. The patient could benefit from imid-based (thalidomide, lenalidomide, pomalidomide) combination chemotherapy once his myeloma progresses or if there is a recurrence of Kaposi's sarcoma.
Assuntos
Mieloma Múltiplo , Sarcoma de Kaposi , Masculino , Humanos , Mieloma Múltiplo/tratamento farmacológico , Mieloma Múltiplo/patologia , Sarcoma de Kaposi/tratamento farmacológico , Sarcoma de Kaposi/patologia , Bortezomib/uso terapêutico , Quimioterapia de Indução , Dexametasona/uso terapêutico , Doença Iatrogênica , Protocolos de Quimioterapia Combinada Antineoplásica/uso terapêuticoRESUMO
A previously healthy man in his 60s being worked up for splenomegaly presented to the emergency department with recurrent episodes of angioedema. Each episode was attributed to a precipitating cause, and consequently, the predisposing C1 esterase inhibitor (C1-INH) deficiency remained undiagnosed until the third presentation. The aetiology of acquired C1-INH deficiency would be primarily obscure and require further investigations to identify. A clonal B cell population was finally isolated by flow cytometry after multiple repeat marrow samples, and a diagnosis of splenic marginal zone lymphoma was subsequently reached. Response to single-agent rituximab was observed with resolution of splenomegaly, disappearance of the antibody and restoration of C1-INH levels.
Assuntos
Angioedema , Neoplasias Hematológicas , Angioedema/diagnóstico , Angioedema/tratamento farmacológico , Angioedema/etiologia , Proteína Inibidora do Complemento C1 , Neoplasias Hematológicas/complicações , Humanos , Masculino , Rituximab/uso terapêutico , Esplenomegalia/complicaçõesRESUMO
INTRODUCTION: Chronic plantar heel pain (CPHP) is a significant, painful condition referring to a range of undifferentiated foot conditions that affect the heel of the foot. METHOD: Participants presenting with CPHP of more than 6 months' duration were recruited on a first through the door basis. Computer-Aided Design and Computer-Aided Manufactured (CAD-CAM) orthoses were designed and constructed for each participant, then dispensed as per normal practice. Pre- and postintervention assessment of pain was performed at baseline and after 6 weeks of use, utilizing the pain subset of the Foot Function Index (FFI). RESULTS: There was a significant reduction in the mean pain scores for all participants in all constructs of the FFI. Total FFI score was also significant ( P = .003). CONCLUSION: CAD-CAM orthoses have the potential to become a treatment modality of choice in CPHP since they have resulted in a significant improvement in heel pain after only 6 weeks' use. LEVELS OF EVIDENCE: Therapeutic, Level IV: Prospective, comparative trial.