1.Recurrent anorexia and pigmentation of skin for more than two months in an infant.
Zhang-Qian ZHENG ; Bing-Bing WU ; Miao-Ying ZHANG ; Wei LU ; Fei-Hong LUO
Chinese Journal of Contemporary Pediatrics 2017;19(8):926-929
A 2-month-old boy presented with adrenal insufficiency, impaired liver function, hypertriglyceridemia, significantly elevated creatine kinase and electrolyte disturbance. Microarray comparative genomic hybridization (aCGH) analysis test showed a pathogenic 8.7 Mb deletion in the short arm of chromosome X (Xp21.3 - p21.1) and confirmed the diagnosis of complex glycerol kinase deficiency (cGKD). He was treated with hydrocortisone, coenzyme Q10 and L-carnitine and was subsequently followed up for 4 years. His serum cortisol levels returned to normal one week later after treatment, but the serum creatine kinase, triglyceride and aminotransferase levels were progressively increased along with mental retardation and decreased muscular strength. cGKD is also named as Xp21 contiguous gene syndrome. The clinical manifestations of this disease include hypertriglyceridemia, congenital adrenal hypoplasia (AHC), Duchenne muscular dystrophy, and mental retardation. This case highlights the necessity to screen the serum triglyceride and creatine kinase levels in infants with suspected adrenal insufficiency.
Anorexia
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etiology
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Comparative Genomic Hybridization
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Humans
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Hypoadrenocorticism, Familial
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complications
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diagnosis
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drug therapy
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Infant
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Male
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Recurrence
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Skin Pigmentation
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Triglycerides
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blood
2.Safety of Megestrol Acetate in Palliating Anorexia-Cachexia Syndrome in Patients with Castration-Resistant Prostate Cancer.
Sungwoo HONG ; In Gab JEONG ; Dalsan YOU ; Jae Lyun LEE ; Jun Hyuk HONG ; Hanjong AHN ; Choung Soo KIM
Journal of Korean Medical Science 2013;28(5):687-692
There are concerns whether megestrol acetate (MA) stimulates the growth of prostate cancer in castration-resistant prostate cancer (CRPC). We evaluated the effect of cumulative doses of MA on the disease-specific survival (DSS) in patients with CRPC who were receiving Docetaxel-based chemotherapy. From July 2003 through June 2009, we identified 109 consecutive patients with CRPC and who had received docetaxel-based chemotherapy. Of these patients, 68 (62.4%) have not received MA, whereas 21 patients (19.3%) and 20 patients (18.3%) had received low dose MA (total < or = 18,400 mg) and high dose MA (total > 18,400 mg), respectively. We assessed the effect of several variables on DSS. None of the clinicopathological variables differed among the three groups. When comparing DSS using Kaplan-Meier analysis, there was no statistically significant survival differences among the three groups (P = 0.546). Using multivariate Cox proportional analyses with backward elimination, the number of docetaxel cycles was only significant factor predicting DSS (HR: 0.578, 95% CI: 0.318-0.923, P = 0.016). Cumulative doses of MA as adjuvant treatment for patients with CRPC and who are receiving docetaxel-based chemotherapy, did not affect their DSS. Therefore, MA can be safely administered in cachexic patients with CRPC.
Aged
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Aged, 80 and over
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Anorexia/complications/*drug therapy
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Antineoplastic Agents/therapeutic use
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Antineoplastic Agents, Hormonal/*therapeutic use
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Cachexia/complications/*drug therapy
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Castration
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Humans
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Kaplan-Meier Estimate
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Male
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Megestrol Acetate/*therapeutic use
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Middle Aged
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Proportional Hazards Models
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Prostatic Neoplasms/complications/*drug therapy/mortality
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Taxoids/therapeutic use