Results 251 to 260 of about 273,677 (294)
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Endocrine Practice, 2013
This review outlines advances in the diagnosis, genetic testing, and progress in medullary thyroid cancer (MTC) treatment in light of the most recent evidence.English-language articles pertaining to MTC published up to 2012 were reviewed. The pertinent articles and their references were obtained and those considered relevant were reviewed for inclusion.
Marcio L, Griebeler +2 more
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This review outlines advances in the diagnosis, genetic testing, and progress in medullary thyroid cancer (MTC) treatment in light of the most recent evidence.English-language articles pertaining to MTC published up to 2012 were reviewed. The pertinent articles and their references were obtained and those considered relevant were reviewed for inclusion.
Marcio L, Griebeler +2 more
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Histiocytic medullary reticulosis
The American Journal of Medicine, 1965Abstract A patient is described with clinical and morphologic features seen in previously reported cases of histiocytic medullary reticulosis and with the unusual antemortem findings of bizarre histiocytes in the blood and bone marrow, as well as skin involvement.
R M, FRIEDMAN, N H, STEIGBIGEL
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Current Treatment Options in Oncology, 2003
Medullary thyroid carcinoma (MTC) is a neuroendocrine malignancy that occurs in hereditary (25%) and sporadic (75%) clinical settings. MTC is present in all patients with the multiple endocrine neoplasia type 2 syndromes. MTCs produce calcitonin, the measurement of which can indicate the presence of tumors in people who are at risk and the ...
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Medullary thyroid carcinoma (MTC) is a neuroendocrine malignancy that occurs in hereditary (25%) and sporadic (75%) clinical settings. MTC is present in all patients with the multiple endocrine neoplasia type 2 syndromes. MTCs produce calcitonin, the measurement of which can indicate the presence of tumors in people who are at risk and the ...
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American Journal of Otolaryngology, 1993
Medullary thyroid carcinoma (MTC) comprises approximately 1–2% of thyroid malignancies and occurs in sporadic and heritable forms. Hereditary forms include multiple endocrine neoplasia (MEN) type 2A, familial medullary thyroid carcinoma (FMTC), and MEN type 2B.
Y L, Colson, S E, Carty
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Medullary thyroid carcinoma (MTC) comprises approximately 1–2% of thyroid malignancies and occurs in sporadic and heritable forms. Hereditary forms include multiple endocrine neoplasia (MEN) type 2A, familial medullary thyroid carcinoma (FMTC), and MEN type 2B.
Y L, Colson, S E, Carty
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Histiocytic Medullary Reticulosis
Australian and New Zealand Journal of Medicine, 1975Summary: The clinical and pathological features of histiocytic medullary reticulosis (HMR) are described in five patients. Treatment by splenectomy and the MOPP routine resulted in a transient improvement in platelet and neutrophil counts and resolution of anaemia and apparent prolongation of survival in two of the five patients.The relationship of ...
J R, Sullivan +3 more
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Computerized Medical Imaging and Graphics, 1989
Two patients developed primary medullary hemorrhages. Both patients were normotensive. They were both receiving oral anticoagulation but the coagulation studies were not excessively prolonged at the time that the hemorrhage occurred. The diagnosis of primary medullary hemorrhage was established by CT findings.
L A, Weisberg +3 more
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Two patients developed primary medullary hemorrhages. Both patients were normotensive. They were both receiving oral anticoagulation but the coagulation studies were not excessively prolonged at the time that the hemorrhage occurred. The diagnosis of primary medullary hemorrhage was established by CT findings.
L A, Weisberg +3 more
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The American Journal of Medicine, 1965
Abstract Twenty cases of medullary sponge kidney (MSK), diagnosed on the basis of urographic findings, are reported in tabular form, the pertinent literature is considered and the generally held concept of MSK as a distinct clinical and pathologic entity is critically examined. The available evidence does not support the distinctiveness of MSK. Rather,
R C, MORRIS +3 more
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Abstract Twenty cases of medullary sponge kidney (MSK), diagnosed on the basis of urographic findings, are reported in tabular form, the pertinent literature is considered and the generally held concept of MSK as a distinct clinical and pathologic entity is critically examined. The available evidence does not support the distinctiveness of MSK. Rather,
R C, MORRIS +3 more
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The British Journal of Radiology, 1962
A case of medullary sponge kidney is presented, as little has been published in the British literature on this subject, apart from a paper by Rubin, Cosbie Ross and Turner (1959), and a case described by Pyrah and Hodgkinson (1960) in a discussion of nephrocalcinosis; the condition is also known as cystic disease of the renal pyramids.
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A case of medullary sponge kidney is presented, as little has been published in the British literature on this subject, apart from a paper by Rubin, Cosbie Ross and Turner (1959), and a case described by Pyrah and Hodgkinson (1960) in a discussion of nephrocalcinosis; the condition is also known as cystic disease of the renal pyramids.
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2011
Abstract Medullary thyroid carcinoma (MTC) is a rare calcitonin-secreting tumour of the parafollicular or C cells of the thyroid. As the C cells originate from the embryonic neural crest, MTC often have the clinical and histological features of neuroendocrine tumours.
Friedhelm Raue, Karin Frank-Raue
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Abstract Medullary thyroid carcinoma (MTC) is a rare calcitonin-secreting tumour of the parafollicular or C cells of the thyroid. As the C cells originate from the embryonic neural crest, MTC often have the clinical and histological features of neuroendocrine tumours.
Friedhelm Raue, Karin Frank-Raue
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Surgical Oncology Clinics of North America, 2006
The goal in managing patients who have MTC is to detect and surgically remove disease at an early stage. Tumor marker-based biochemical screening and DNA-based genetic screening have created the opportunity for effective prophylactic surgery in patients at risk for hereditary MTC.
Y Nancy, You +3 more
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The goal in managing patients who have MTC is to detect and surgically remove disease at an early stage. Tumor marker-based biochemical screening and DNA-based genetic screening have created the opportunity for effective prophylactic surgery in patients at risk for hereditary MTC.
Y Nancy, You +3 more
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