RESUMO
OBJECTIVE: We aim to report a case of Kaposi sarcoma (KS) with Cushing's syndrome caused by endogenic glucocorticoid-induced immunosuppression. CLINICAL PRESENTATION: A 43-year-old woman presented with delirium, hirsutism, fatigue, and hypertension. At the time of presentation, physical findings showed a Cushingoid appearance, with moon-like facies, hirsutism, and hyperpigmentation. Laboratory findings showed the following: adrenocorticotropic hormone, 86.7 pg/mL (normal range, 0-46 pg/mL); baseline cortisol level, 50 microg/dL (normal range, 6.2-19 microg/dL); potassium, 2.2 mEq/L (normal range, 3.5-5 mEq/L); and midnight cortisol level, 33 microg/dL. Serum cortisol levels failed to suppress after low and high doses of dexamethasone; these findings confirmed the diagnosis of ectopic adrenocorticotropic hormone production. Magnetic resonance imaging revealed a 12 x 15-mm, round, hypothalamic mass lesion in the center of the median eminence. INTERVENTION: Endoscopic biopsy from the floor of the third ventricle was performed, and pathological examination of the lesion showed a diffuse adrenocorticotropic hormone-secreting adenoma. The patient developed diffuse skin lesions that were proven to be a KS by skin biopsy while she was prepared for transcranial surgery. After surgical removal of the adenoma, she became hypocortisolemic and required cortisol replacement. Within 1 month after surgery, all KS lesions disappeared spontaneously. CONCLUSION: Excessive cortisol may induce immunosuppression. KS is one of the most common malignant tumors of patients with immunosuppression. To the best of our knowledge, this is the first case of Cushing's syndrome with KS caused by endogenous glucocorticoid-induced immunosuppression.
Assuntos
Síndrome de ACTH Ectópico/imunologia , Adenoma/metabolismo , Hormônio Adrenocorticotrópico/metabolismo , Neoplasias Hipotalâmicas/metabolismo , Neoplasias Hipofisárias/metabolismo , Sarcoma de Kaposi/imunologia , Síndrome de ACTH Ectópico/patologia , Síndrome de ACTH Ectópico/fisiopatologia , Adenoma/patologia , Adenoma/cirurgia , Hormônio Adrenocorticotrópico/sangue , Adulto , Coristoma/patologia , Coristoma/fisiopatologia , Coristoma/cirurgia , Síndrome de Cushing/complicações , Síndrome de Cushing/imunologia , Síndrome de Cushing/fisiopatologia , Feminino , Humanos , Hidrocortisona/sangue , Neoplasias Hipotalâmicas/patologia , Neoplasias Hipotalâmicas/cirurgia , Hipotálamo/metabolismo , Hipotálamo/patologia , Hipotálamo/cirurgia , Tolerância Imunológica/imunologia , Hospedeiro Imunocomprometido/imunologia , Imageamento por Ressonância Magnética , Eminência Mediana/metabolismo , Eminência Mediana/patologia , Eminência Mediana/cirurgia , Procedimentos Neurocirúrgicos , Neoplasias Hipofisárias/patologia , Neoplasias Hipofisárias/cirurgia , Sarcoma de Kaposi/patologia , Sarcoma de Kaposi/fisiopatologia , Resultado do TratamentoRESUMO
Ilustramos el caso de un paciente de 40 años de edad, sexo masculino, homosexual, con sarcoma de kaposi gastrointestinal sin lesiones cutáneas como primera manifestación de SIDA, quien presentaba lesión en el dorso de la lengua de aspecto polipoide y violácea asociada a pólipos rectales. Se realizaron estudios de vías digestivas altas y colon enema de doble contraste los cuales evidenciaron lesiones nodulares son umbilicación central y compresiones extrínsecas en la mayor parte del tracto gastrointestinal. Se confirmó diagnostico de sarcoma de kaposi mediante biopsia de las lesiones.El reporte de este caso único quiere ilustrar la presentación radiológica del sarcoma de Kaposi en el tracto gastrointestinal sin compromiso cutáneo y como primera manifestación de SIDA.
Assuntos
Humanos , Infecções Oportunistas Relacionadas com a AIDS/diagnóstico , Infecções Oportunistas Relacionadas com a AIDS/etiologia , Infecções Oportunistas Relacionadas com a AIDS/fisiopatologia , Sarcoma de Kaposi/diagnóstico , Sarcoma de Kaposi/etiologia , Sarcoma de Kaposi/fisiopatologia , Síndrome da Imunodeficiência Adquirida/complicaçõesRESUMO
Secretion of angiogenesis inhibitors and stimulators is modulated during in vitro differentiation of embryonic chick growth plate chondrocytes. Supernatants from dedifferentiated cells undergoing maturation to hypertrophic chondrocytes in suspension progressively inhibited vascular cell random migration and invasion of basement membrane matrix by endothelial cells. Maximal inhibition was exhibited by conditioned medium from hypertrophic chondrocytes. The same medium also repressed vascular cell migration induced by highly angiogenic Kaposi's sarcoma cell supernatants and prevented formation of an anastomosed network of tube-like structures by endothelial cells plated on matrigel. On the contrary, when the suspension culture of hypertrophic chondrocytes was supplemented with ascorbic acid, a condition leading to the formation of a mineralized tissue similar to calcified cartilage, a dramatic switch to production of angiogenic activity was observed. Medium conditioned by osteoblast-like cells derived from hypertrophic chondrocytes also induced vascular cell migration and invasion of basement membrane matrix. The presence of angiogenic activity in the conditioned medium was assessed also by an in vivo assay in mice using reconstituted basement membrane associated with heparin. Therefore, interactions of chondrocytes with their extracellular matrix are an absolute requirement for the expression of angiogenic activities by hypertrophic chondrocytes at late developmental stages.