We studied the effects of L-carnitine on growth performance, carcass composition, and lipid metabolism in male broilers. Six hundred male commercial broilers were allotted to five groups, each of which included three replicates (40 birds per replicate). The groups received the same basal diet supplemented with 0, 25, 50, 75, or 100 mg/kg L-carnitine, respectively. The feeding trial showed that L-carnitine had no significant effect on daily gain or feed conversion. Supplementation with L-carnitine (above 25 mg/kg) in the diet increased breast muscle yield (P < 0.05) and crude fat content of the muscles and decreased abdominal fat content (P < 0.05). Addition of 50, 75, or 100 mg/kg L-carnitine to the diet decreased total activities of glucose-6-phosphate dehydrogenase, malic dehydrogenase, isocitrate dehydrogenase, and lipoprotein lipase (P < 0.05) in the subcutaneous fat and total activity of carnitine palmitoyltransferase-I (P < 0.05) in breast muscles. The results of this study indicate that L-carnitine could reduce the deposit of subcutaneous fat by decreasing total activities of enzymes in the fat and enhance intramuscular fat by decreasing the activity of carnitine palmitoyltransferase-I in breast muscles.

Our study further confirms that C-RDD is a distinct entity with different age and possibly race distributions from RDD. Compared with its nodal counterpart, C-RDD demonstrates a wider histopathological spectrum with different clinicopathological phases depending on duration of the lesions. Awareness of these features is helpful in making a correct diagnosis. The associations of C-RDD with other histiocytoses may have important implications for the pathogenesis of this rare histiocytosis.

This basic study has encouraged the further investigation of ALA permeation by laser or microdermabrasion.

Rosai-Dorfman disease (RDD; sinus histiocytosis with massive lymphadenopathy) and Langerhans cell histiocytosis (LCH) are two different yet pathogenetically related histiocytic disorders. While systemic and localized forms have been identified in both diseases, each has its own characteristic histological, immunohistochemical and ultrastructural profile. Rarely, either RDD or LCH can also occur in the context of certain malignant neoplasms. However, the coexistence of RDD and LCH has never been described. We report a case of cutaneous RDD in which a focus of LCH was found. Clinical and laboratory examinations revealed no evidence of extracutaneous involvement of RDD or LCH. We believe that this is the first report of such a coexistence, and the possible pathogenesis is discussed.

Fusarium oxysporum f. sp. cubense (Foc) causes Fusarium wilt, a lethal disease that results in devastating economic losses to banana production worldwide. The pathogen originates from Asia where it evolved with its host, the wild banana plant Musa acuminata. Foc consists of three races, eight lineages and 24 Vegetative Compatibility Groups (VCGs). Most damage is caused by Foc tropical race 4 (TR4), which occurs exclusively in Asia. China is the biggest producer of Cavendish bananas (AAA) in the world, with plantations covering approximately 372.4677×10 3 hectares constituting up 90% of banana production, with the rest made up of Pisang Awak (ABB) and Dajiao or Plantain (AAB) bananas. In this study, 80 Foc isolates from six production areas were collected from diseased banana cultivars in China. These isolates were all single-spored and characterized to lineage level using five restriction enzymes while VCG identity was determined by generating nit-mutants, and pairing these mutants with a VCG tester set for Foc. To determine the occurrence of Foc TR4 in China, all isolates were screened with a newly developed Foc TR4-specific primer set. All the Foc isolates were also inoculated on Cavendish, Pisang Awak and Dajiao bananas for pathogenicity testing. Our results showed that Foc in China was highly diverse, as five of the eight lineages and 11 of the 24 known VCGs could be determined. The Foc TR4-specific primer set was highly specific for detecting VCG 01213/16, and could be used in diversity studies to rapidly identify this VCG complex. The majority of the isolates from China were identified as Foc TR4 (VCG 01213/16), and this VCG was found in four of the five production areas. Species of Fusarium other than F. oxysporum were non-pathogenic to banana. The selection of Foc-resistant banana clones, and the development of appropriate disease management strategies for Fusarium wilt of banana in China, is urgently required.

Acute myeloid leukemia (AML) with minimal differentiation was usually referred to as acute undifferentiated leukemia in the past. With the help of immunophenotyping, this subtype of leukemia was shown to express myeloid antigens on the blasts and was designated AML-M0 by FAB Cooperative Study Group in 1991. Among the 423 consecutive newly diagnosed de novo AML at our institution, 12 (2.8%) were of M0 subtype. The proportion of M0 in AML was higher in children than in adults (8.2% vs 1.7%). Four other M0 patients referred from outside hospitals for immunophenotyping were also included in this study. There were two peaks in age distribution of these 16 patients: less than 3 years and between 51 and 70 years, respectively. Organomegaly was more common in patients with AML-M0 than in those with other subtypes (56.3% vs 29.2%, P = 0.025). The former patients had higher incidences of CD7 and CD34 expression on the leukemic cells than the latter ones (50% vs 16.9%, P = 0.003 and 69.2% vs 37.9%, P = 0.019, respectively). The patients with AML-M0 showed more frequent clonal chromosomal abnormalities in the leukemic cells than other AML patients (83.3% vs 53.9%, P = 0.039); the same is also true for complex cytogenetic aberrations (50% vs 11.4%, P = 0.004). Adults with AML-M0 showed a lower complete remission (CR) rate and significantly poorer survival than those with non M0-AML. However there was no significant difference in outcome between the two groups of pediatric patients. In conclusion, AML-M0 is a unique subtype of leukemia that has distinct age distribution and shows different clinical and biological characteristics from other AML. Adult patients have poor prognosis. Whether pediatric patients had better outcome than adults needs to be clarified in further studies.

4 Ichimima M, Hamamoto Y, Muto M. A case of baboon syndrome associated with group A streptococcal infection. J Dermatol 2003; 30: 69-71.Cutaneous hyalohyphomycosis caused by Acremonium in an immunocompetent patient

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