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1.
Acta Endocrinol (Buchar) ; 12(1): 80-84, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-31258806

RESUMO

The thyroid gland is one of the most vascularized organs in the body. However, metastatic disease to the thyroid gland is rare. When it does occur kidney is the most common primary tumor site, followed by melanoma, lung, breast, esophagus, uterus and colon carcinoma. We describe the case of an isolated thyroid metastasis from clear cell renal carcinoma occurring 16 years after nephrectomy. An 82 years-old woman presented for the recent growth of a right thyroid nodule, diagnosed 3 years before, when a fine needle aspiration biopsy found a benign cytology suggesting a well-differentiated follicular thyroid adenoma. Her medical history included type 2 diabetes mellitus, atrial fibrillation and a right nephrectomy for a clear cell renal carcinoma done 16 years before. The patient has lost weight but she was otherwise asymptomatic. The right lobe goiter was painless, firm, and mobile with deglutition, without signs of local compression or latero-cervical lymphadenopathy. Thyroid ultrasonography revealed an enlarged (9.9 cm) macronodular right lobe, with multiple cystic areas, with normal left lobe and a thrombus in the right internal jugular vein. Thyroid function tests were normal. The patient was suspected of thyroid carcinoma and underwent a near total thyroidectomy. Histopathological examination revealed a metastasis of clear cell renal carcinoma in the right thyroid gland lobe (8.5/5/5 cm). Further imaging showed no primary tumor or other metastases. Metastatic renal carcinoma to the thyroid should be considered in any patient presenting with a thyroid mass and a medical history of operated renal cell carcinoma, since it can occur up to 25 years after nephrectomy.

2.
J Med Life ; 8(1): 106-8, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-25914751

RESUMO

Cystic lesions of the pancreas are relatively rare entities but have been increasingly diagnosed in recent years due to advanced imaging techniques. This category encompasses pancreatic pseudocyst as well as a wide range of pancreatic tumors with benign behavior, borderline or primary malignant. Serous cystadenoma of the pancreas represents the most common benign pancreatic tumor, with a very low but well recognized malignant potential. The clinical presentation varies according to its size; small tumors may be asymptomatic and discovered incidentally, while large tumors are more likely symptomatic. We report the case of a female patient presenting with non-specific left abdominal pain, who was diagnosed through a CT scan with a caudal pancreatic tumor. The patient underwent spleen-preserving distal pancreatectomy. The result of the histopathological examination revealed a serous cystadenoma.


Assuntos
Cistadenoma Seroso/patologia , Neoplasias Pancreáticas/patologia , Baço/patologia , Cistadenoma Seroso/diagnóstico por imagem , Cistadenoma Seroso/cirurgia , Feminino , Humanos , Pessoa de Meia-Idade , Pancreatectomia , Neoplasias Pancreáticas/diagnóstico por imagem , Neoplasias Pancreáticas/cirurgia , Baço/diagnóstico por imagem , Tomografia Computadorizada por Raios X
3.
J Med Life ; 7 Spec No. 4: 99-102, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-27057259

RESUMO

Celiac disease is a complex disorder characterized by digestive symptoms as well as extraintestinal manifestations, sometimes difficult to diagnose. Commonly described as a disease of childhood, adult celiac disease is a well known entity that should be taken into the differential diagnosis of a chronic diarrhea or of a malabsorption syndrome. The pathogenesis encompasses an autoimmune pathway that acts on a genetic background. The mucosa of the small intestine became damaged in reponse to foods that contain gluten in subjects with genetic susceptibility. The clinical presentation is variable, ranging from typical gastrointestinal symptoms to extradigestive and systemic manifestations. The simple withdrawal of the dietary gluten results in clinical improvement and healing of the intestinal mucosa. We report the case of an young women diagnosed with celiac disease after 7 years of iron deficiency anemia without a clear etiology.


Assuntos
Anemia Ferropriva/complicações , Doença Celíaca/complicações , Adulto , Complexo CD3/metabolismo , Antígenos CD8/metabolismo , Doença Celíaca/patologia , Endoscopia Gastrointestinal , Feminino , Humanos , Imuno-Histoquímica , Linfócitos T/patologia
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