Subject(s)
Angiogenesis Inhibitors/adverse effects , Antibodies, Monoclonal/adverse effects , Fibrosarcoma/secondary , Glomerulonephritis, Membranoproliferative/chemically induced , Lung Neoplasms/secondary , Adult , Angiogenesis Inhibitors/therapeutic use , Antibodies, Monoclonal/pharmacology , Antibodies, Monoclonal/therapeutic use , Antibodies, Monoclonal, Humanized , Antineoplastic Combined Chemotherapy Protocols/administration & dosage , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Bevacizumab , Bowman Capsule/blood supply , Bowman Capsule/physiology , Dacarbazine/administration & dosage , Deoxycytidine/administration & dosage , Deoxycytidine/adverse effects , Deoxycytidine/analogs & derivatives , Disease Progression , Docetaxel , Doxorubicin/administration & dosage , Endothelium, Vascular/drug effects , Endothelium, Vascular/physiopathology , Fibrosarcoma/drug therapy , Fibrosarcoma/surgery , Humans , Ifosfamide/administration & dosage , Lung Neoplasms/drug therapy , Male , Mesna/administration & dosage , Muscle Neoplasms/drug therapy , Muscle Neoplasms/surgery , Podocytes/physiology , Proteinuria/chemically induced , Taxoids/administration & dosage , Vascular Endothelial Growth Factor A/antagonists & inhibitors , Vascular Endothelial Growth Factor A/physiology , GemcitabineABSTRACT
Fanconi Syndrome is characterized by a transport defect in the proximal tubules, complete or partial, leading to reabsorption and secretion defect of amino acids, glucose, bicarbonates and other organic compounds. Associated with numerous disease states ranging from rare inherited disorders of metabolism to exposure to exogenous toxins. We report a case of acute renal failure and tubulopathy after burns caused by toxic metals agents.
Subject(s)
Accidents, Occupational , Burns, Chemical/complications , Cadmium/toxicity , Fanconi Syndrome/chemically induced , Lead/toxicity , Humans , Male , Young AdultABSTRACT
No disponible
Subject(s)
Humans , Male , Young Adult , Fanconi Syndrome/diagnosis , Burns, Chemical/complications , Cadmium Poisoning/complications , Lead Poisoning/complicationsABSTRACT
Una mujer de 53 años fue remitida a nuestra consulta para un estudio de hipertensión. Se detectó elevación de catecolaminas, metanefrinas y vanilmandélico en orina. En tomografía axial computarizada abdominal se demostró un nódulo suprarrenal de 3,3 cm, compatible todo ello con feocromocitoma. Cuatro meses después la paciente consulta por un cuadro de diarrea acuosa y pérdida de peso. Tras la realización de adrenalectomía laparoscópica remitió el cuadro de diarrea. Ante la sospecha de vipoma (tumor secretor de péptido intestinal vasoactivo [VIP]) se procedió a la realización de VIP en la pieza quirúrgica mediante técnicas inmunohistoquímicas; el resultado fue positivo. El diagnóstico final fue de feocromocitoma secretor de VIP
A 53 year-old woman referred to our consultation for study of hypertension. Catecholamines, metanephrines and vanilmandelic acid in urine was detected. Abdominal CT scan demonstrated a 3.3 cm adrenal node, all with pheochromocytoma. Months after, the patient consulted for a picture of watery diarrhea and weight loss. After performing laparoscopic adrenalectomy, the diarrhea picture remitted. Due to the suspicion of vipoma (VIP secreting tumor), vasoactive intestinal peptide (VIP) was visualized in surgical pieces using immunohistochemical techniques, this being positive. The final diagnosis was VIP secreting pheochromocytoma
Subject(s)
Humans , Male , Middle Aged , Hypertension/complications , Diarrhea/complications , Pheochromocytoma/pathology , Vipoma/pathology , Vasoactive Intestinal Peptide/analysisABSTRACT
No disponible