2.Clinical characteristics and prognostic factors of malignancy-associated hypercalcemia in squamous cell carcinoma.
Su-jie ZHANG ; Yi HU ; Shun-chang JIAO ; Zhe-feng LIU ; Hai-tao TAO
Acta Academiae Medicinae Sinicae 2012;34(6):585-589
OBJECTIVETo explore the clinical characteristics and prognostic factors of patients diagnosed with squamous cell carcinoma (SCC) and presented malignancy-associated hypercalcemia (MAH).
METHODSWe retrospectively analyzed the clinical data of 36 patients with biopsy-proven SCC and presented MAH who were treated at the our department from January 2001 to December 2010. The survival were analyzed using the Kaplan-Meier method and Cox analysis.
RESULTSAmong these 36 patients, the median blood calcium level was 2.94 mmol/L (2.77-4.87 mmol/L), and the median survival time was only 45 days (1-839 d). Log-rank test showed that central nervous system symptoms, bone metastasis, and hypercalcemia occurring over 160 days after cancer diagnosis were predictors for poor survival(p=0.003, P=0.049, P=0.005). In the COX proportional hazard model analysis, central nervous system symptoms and hypercalcemia occurring over 160 days after cancer diagnosis were independent prognostic factors for survival time (RR=5.721, P=0.000; RR=4.624, P=0.001).
CONCLUSIONSPatients with squamous cell carcinoma (SCC) and presented MAH have poor prognosis. Central nervous system symptoms and hypercalcemia occurring over 160 days after cancer diagnosis are independent predictors of the prognosis.
Adult ; Aged ; Carcinoma, Squamous Cell ; complications ; Female ; Humans ; Hypercalcemia ; etiology ; Male ; Middle Aged ; Prognosis ; Retrospective Studies
3.Efficacy of miacalcic in treating a hypercalcemia crisis caused by Williams-Beuren syndrome.
Yi GU ; Chunxiu GONG ; Ying SHEN ; Di WU ; Xuejun LIANG ; Bo CHANG ; Ying LIU ; Yi WANG
Chinese Medical Journal 2014;127(13):2548-2549
4.A case of primary hyperparathyroidism with hypercalcemic nephropathy in children.
Jae Myung YU ; Heui Jung PYO ; Dong Seop CHOI ; Kang Woo LEE ; Kee Hwan YOO ; Chong Suk KIM
Journal of Korean Medical Science 1994;9(3):268-272
Primary hyperparathyroidism is a rare disease in children and is characterized by conspicuous skeletal and renal changes. A 12 year old male patient presented with symptoms of polydipsia, polyuria, general weakness, nausea, and vomiting which had begun 3 months earlier, and showed typical laboratory findings of primary hyperparathyroidism. Confirmatory diagnosis was made by elevated parathyroid hormone concentration in serum, technetium-thallium subtraction scan imaging method and histopathologic finding of chief cell hyperplasia. The laboratory findings revealed elevated levels of BUN, creatinine and decreased GFR. Kidney biopsy showed typical calcium deposits in tubules with marked tubulointerstitial infiltration. After subtotal parathyroidectomy, clinical findings improved remarkably.
Case Report
;
Child
;
Human
;
Hypercalcemia/*etiology
;
Hyperparathyroidism/*complications/pathology
;
Hyperplasia
;
Kidney/pathology
;
Kidney Diseases/*etiology
;
Male
;
Parathyroid Glands/pathology
5.Technetium-99m MDP bone scintigraphic findings of hypercalcemia in accelerated phase of chronic myelogenous leukemia.
Hyo Sung KWAK ; Myoung Hee SOHN ; Seok Tae LIM ; Jae Yong KWAK ; Chang Yeol YIM
Journal of Korean Medical Science 2000;15(5):598-600
Hypercalcemia in accelerated phase of chronic myelogenous leukemia (CML) is very rare. Its pathogenesis is considered humoral hypercalcemia of malignancies mediated by parathyroid hormone-related protein (PTHrP). In severe hypercalcemia, calcifications in kidneys, skin, vessels, heart, and stomach may occur. Our two cases were admitted because of severe hypercalcemia in accelerated phase of CML. On Tc-99m methylene diphosphonate (MDP) bone scintigraphies, a marked tracer accumulation was seen in the lung, heart, stomach and kidney. We report increased tracer accumulation of multiple organs on Tc-99m MDP bone scintigraphy in two rare hypercalcemic patients with CML.
Adult
;
Bone Diseases/radionuclide imaging*
;
Bone Diseases/etiology*
;
Calcinosis/radionuclide imaging
;
Calcinosis/etiology
;
Case Report
;
Human
;
Hypercalcemia/radionuclide imaging*
;
Hypercalcemia/etiology*
;
Leukemia, Myeloid, Chronic/metabolism
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Leukemia, Myeloid, Chronic/complications*
;
Male
;
Middle Age
;
Proteins/metabolism
;
Technetium/diagnostic use
6.Inadvertent haemodialysis in a pulmonary tuberculosis patient with hypercalcaemia.
Chai Soon NGIU ; Chee Yean LOO ; Andrea Y L BAN ;
Annals of the Academy of Medicine, Singapore 2010;39(5):415-416
Cachexia
;
etiology
;
Cough
;
Delayed Diagnosis
;
Fever
;
Humans
;
Hypercalcemia
;
etiology
;
Male
;
Middle Aged
;
Radiography
;
Renal Dialysis
;
Renal Insufficiency
;
etiology
;
therapy
;
Tuberculosis, Pulmonary
;
complications
;
diagnostic imaging
8.Severe hypercalcemia complicated in acute lymphoblastic leukemia (ALL) with E2A-HLF fusion gene: report of two cases and literature review.
Jun YANG ; Xuan ZHOU ; Bin WANG ; Chao GAO ; Rui-dong ZHANG ; Bin LI
Chinese Journal of Hematology 2009;30(9):615-618
OBJECTIVETo improve the understanding of severe hypercalcemia complicated in acute lymphoblastic leukemia (ALL) with E2A-HLF fusion gene, and to explore the mechanism of pathogenesis and the relationship between the special gene translocation and severe hypercalcemia.
METHODSTwo patients with severe hypercalcemia complicated in ALL were reported.
RESULTSTwo patients with E2A-HLF fusion gene, which is generated by t(17;19) (q22, p13) translocation, suffered relapse of leukemia three months after chemotherapy, and developed severe hypercalcemia. After further chemotherapy, the hypercalcemia symptoms were corrected or alleviated.
CONCLUSIONSevere hypercalcemia is one of rare complications of ALL. In B cell lymphoblastic leukemia with E2A-HLF fusion gene, the fusion gene showed be closely monitored for evaluating the disease situation.
Child ; DNA-Binding Proteins ; genetics ; Female ; Humans ; Hypercalcemia ; etiology ; genetics ; Infant ; Male ; Oncogene Proteins, Fusion ; genetics ; Precursor Cell Lymphoblastic Leukemia-Lymphoma ; complications ; genetics ; Prognosis ; Transcription Factors ; genetics
10.Atypical Radiological Manifestation of Pulmonary Metastatic Calcification.
Eun Hae KANG ; Eun Sun KIM ; Chul Hwan KIM ; Soo Youn HAM ; Yu Whan OH
Korean Journal of Radiology 2008;9(2):186-189
Metastatic pulmonary calcification refers to calcium deposition in the normal pulmonary parenchyma and this deposition is secondary to abnormal calcium metabolism. The most common radiologic manifestation consists of poorly-defined nodular opacities that are mainly seen in the upper lung zone. We present here a case of metastatic pulmonary calcification that manifested as atypical, dense, calcium deposition in airspaces within the previously existing consolidation in the bilateral lower lobes, and this process was accelerated by pneumonia-complicated sepsis in a patient with hypercalcemia that was due to hyperparathyroidism.
Calcinosis/*radiography
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Female
;
Humans
;
Hypercalcemia/etiology
;
Hyperparathyroidism/complications/surgery
;
Lung Diseases/*radiography
;
Middle Aged
;
Parathyroidectomy
;
Pneumonia/complications
;
Shock, Septic/microbiology
;
Tomography, X-Ray Computed/methods