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1.
Pediatr Transplant ; 16(7): E320-4, 2012 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-22404497

RESUMEN

PTLD is a serious and frequently observed complication after solid organ transplantation. We present a six-yr-old girl with a rapidly growing, solid tumor of the lip four yr after orthotopic heart transplantation, which was classified as monomorphic PTLD with the characteristics of a diffuse large B-cell lymphoma. Treatment with reduction in immunosuppression, ganciclovir, and anti B-cell monoclonal antibody (rituximab) resulted in full remission since 12 months. To the best of our knowledge, this report is the first description of PTLD in the lip in a pediatric patient after heart transplantation in the English literature.


Asunto(s)
Cardiomiopatías/terapia , Insuficiencia Cardíaca/terapia , Trasplante de Corazón/efectos adversos , Neoplasias de los Labios/etiología , Labio/inmunología , Linfoma de Células B/complicaciones , Trastornos Linfoproliferativos/diagnóstico , Anticuerpos Monoclonales de Origen Murino/farmacología , Cardiomiopatías/complicaciones , Niño , Infecciones por Virus de Epstein-Barr/complicaciones , Infecciones por Virus de Epstein-Barr/diagnóstico , Femenino , Ganciclovir/farmacología , Insuficiencia Cardíaca/complicaciones , Herpesvirus Humano 4/metabolismo , Humanos , Inmunosupresores/farmacología , Neoplasias de los Labios/terapia , Linfoma de Células B/terapia , Trastornos Linfoproliferativos/complicaciones , Complicaciones Posoperatorias , Inducción de Remisión , Rituximab , Factores de Tiempo
2.
Eur J Med Res ; 16(11): 491-4, 2011 Nov 10.
Artículo en Inglés | MEDLINE | ID: mdl-22027642

RESUMEN

Pyoderma gangrenosum is a non-infectious neutro?philic skin disease commonly associated with underlying systemic diseases. Histopathological and laboratory diagnostics are unspecific in the majority of the cases and the diagnosis is made in accordance with the clinical picture. Here, we report the case of a 69-year old man with progredient pyoderma gangrenosum-like ulcerations under treatment with sunitinib due to hepatocellular carcinoma. A conventional ulcer therapy did not lead to a regression of the lesions. Solely cessation of sunitinib therapy resulted in an improvement of the ulcerations. Sunitinib is a multikinase inhibitor that targets the PDGF-α- and ?ß-, VEGF-1-3-, KIT-, FLT3-, CSF-1- and RET-receptor, thereby impairing tumour proliferation, pathological angiogenesis and metastasation. Here, we demonstrate that pyoderma gangrenosum-like ulcers may represent a serious side effect of sunitinib-based anti-cancer treatment.


Asunto(s)
Antineoplásicos/efectos adversos , Indoles/efectos adversos , Piodermia Gangrenosa/inducido químicamente , Piodermia Gangrenosa/complicaciones , Pirroles/efectos adversos , Úlcera/inducido químicamente , Úlcera/complicaciones , Anciano , Eritema/inducido químicamente , Eritema/complicaciones , Humanos , Hiperpigmentación/inducido químicamente , Hiperpigmentación/complicaciones , Hipopigmentación/inducido químicamente , Hipopigmentación/complicaciones , Masculino , Terapia de Presión Negativa para Heridas , Piodermia Gangrenosa/terapia , Sunitinib , Úlcera/terapia
3.
Hautarzt ; 60(10): 783-7, 2009 Oct.
Artículo en Alemán | MEDLINE | ID: mdl-19756436

RESUMEN

A 68-year-old women with polycythemia vera was treated with hydroxyurea for 8 years and developed painful ulcers on her lower legs, multiple hypertrophic actinic keratoses and a squamous cell carcinoma. After discontinuing hydroxyurea therapy the leg ulcers resolved within 8 weeks. The hypertrophic actinic keratoses and squamous cell carcinoma were treated with cryotherapy and excision, respectively. Hydroxyurea induces a variety of cutaneous side effects such as painful leg ulcers and squamous cell carcinomas. Given the wide variety of adverse cutaneous side effects associated with long-term hydroxyurea therapy, the first step in management is to insure that physicians and patients are aware of the specific risks of this treatment. Patients under hydroxyurea therapy should be monitored closely by dermatologists to early detect and treat the cutaneous side effects.


Asunto(s)
Carcinoma de Células Escamosas/inducido químicamente , Erupciones por Medicamentos/diagnóstico , Hidroxiurea/efectos adversos , Úlcera de la Pierna/inducido químicamente , Úlcera de la Pierna/diagnóstico , Neoplasias Cutáneas/inducido químicamente , Anciano , Antidrepanocíticos/efectos adversos , Antidrepanocíticos/uso terapéutico , Carcinoma de Células Escamosas/diagnóstico , Erupciones por Medicamentos/etiología , Femenino , Humanos , Hidroxiurea/uso terapéutico , Policitemia Vera/complicaciones , Policitemia Vera/tratamiento farmacológico , Neoplasias Cutáneas/diagnóstico
4.
Hautarzt ; 60(4): 278-81, 2009 Apr.
Artículo en Alemán | MEDLINE | ID: mdl-19300913

RESUMEN

Eosinophilic fasciitis is a rare disease characterized by edema, painful indurations, and progressive muscle weakness. Mainly the extremities are involved. We report on a 22-year-old woman with eosinophilic fasciitis presenting with progressive muscle weakness of both hands and feet and a reduced general condition. She showed symmetrical and firm swelling of the extremities with painful restriction of joint movement. Systemic treatment with glucocorticosteroids as well as physiotherapy and manual lymphatic drainage led to continuous improvement of her symptoms. The differentiation from other diseases, such as systemic scleroderma, eosinophilia-myalgia syndrome, and pseudoscleroderma, might be difficult at the beginning of the disease. The gold standard for diagnosis is--as was done in our case--a deep skin-to-muscle biopsy. Further imaging, especially magnetic resonance imaging, can support the diagnostic procedure.


Asunto(s)
Eosinofilia/patología , Fascitis/patología , Espectroscopía de Resonancia Magnética , Debilidad Muscular/diagnóstico , Piel/patología , Femenino , Humanos , Síndrome , Adulto Joven
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