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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    British journal of dermatology 127 (1992), S. 0 
    ISSN: 1365-2133
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Summary Epidermolysis bullosa acquisita (EBA) is a rare acquired subepidermal blistering disorder associated with autoimmunity to type VII collagen. Although the full clinical spectrum of EBA is still being defined, it is now known that EBA has greater clinical heterogeneity than previously suggested. We describe a patient with EBA which closely approximated the severity of the recessive form of dystrophic epidermolysis bullosa.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    International journal of dermatology 36 (1997), S. 0 
    ISSN: 1365-4632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: A 67-year-old Japanese man had been treated occasionally for asthma by oral administration of prednisolone at a dose between 5 and 15 mg/day for 18 years. In December 1993, the patient had a severe asthma attack, during which he developed a pneumothorax, complicated by pneumonia. He was hospitalized immediately, and antibiotics and hydrocortisone were administered intravenously. The treatment was, however, ineffective and his condition deteriorated. In February 1994, he was treated with pulse therapy of 1 g/day of sodium hydrocortisone for 3 days. During the pulse therapy, erythema and red papules were noticed on his right dorsum manus. The erythema progressed with purpura, induration, and local fever. The papules became necrotic, giving rise to small ulcers with effusions (Fig. 1). The patient also developed a subcutaneous nodule on the proximal region of his forearm.Laboratory investigations revealed anemia (hemoglobin (Hb), 9.6 g/dL), leucocytosis (leukocyte count, 11,800/mm3), slight liver dysfunction (GOT 32KU, GPT 71KU, LDH 759UU), and hypoaluminemia (albumin (Alb), 2.7 mg/dL). A biopsy of the indurated erythema of the dorsum manus was performed.The histopathology of the biopsied tissue showed diffuse infiltration with inflammatory cells, edema, and necrosis in the mid-dermis and fat. The infiltrate consisted of lymphocytes, neutrophils, histiocytes, and occasional giant cells. Many mycelial form fungal elements were observed (Fig. 2a), and aggregates of hyphae were also found in the lower dermis (Fig. 2b). Similar findings were noted for the biopsied specimen of the forearm subcutaneous nodule.Biopsied material was inoculated on Sabouraud's dextrose agar, and floccose and smoky-gray colonies grew rapidly at room temperature for 7 days (Fig. 3a). Microscopic findings showed that the hyphae were broad, branching, and brown in color. Round or oval conidia were produced singly on short conidiophores from the sides of the hyphae, or terminally on long conidiophores (Fig. 3b). Scanning electron microscopy showed an oval conidium produced from the terminus of the conidiophore with annellation. Although we observed the cultured mycelium for several months, cleistothecia were not produced. From these findings, we identified the organism as Scedosporium apiospermum, the asexual stage of Pseudallescheria boydii. The organism was not isolated from sputum or blood cultures.The patient was given fluconazole intravenously at 400 mg/day. Although the treatment was stopped after 2 weeks, because of increasing serum transaminase, the erythema and subcutaneous nodule almost completely disappeared after 5 weeks.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    International journal of dermatology 29 (1990), S. 0 
    ISSN: 1365-4632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: A 60-year-old man who had had a renal transplantation developed a nodule on the dorsum of his right middle finger, which was subsequently diagnosed as cutaneous phaeohyphomycosis caused by Exophiala jeanselmei. The patient was successfully treated with 5–fluorocytosine. To our knowledge, this case is the third reported case in the world caused by this species in a postrenal transplant patient that manifested as phaeohyphomycosis.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    International journal of dermatology 32 (1993), S. 0 
    ISSN: 1365-4632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Archives of dermatological research 288 (1996), S. 258-261 
    ISSN: 1432-069X
    Keywords: Key words Apoptosis ; Basal cell carcinoma ; TUNEL
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-069X
    Keywords: Epidermolysis bullosa simplex ; Keratin ; PCR ; Mutation ; PASA method
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Recent advances in molecular biology have enabled the association of epidermolysis bullosa simplex (EBS) with point mutations of keratin 14 and/or keratin 5 genes to be established. We describe here the detection of point mutations in genomic DNA from formalin-fixed and paraffin-embedded sections from five cases of epidermolysis bullosa using the PCR amplification of specific alleles (PASA) method. In two of four cases of Köbner-type EBS a point mutation of helix 2b (384 Leu-Pro) was detected and in one case of Dowling-Meara-type EBS a mutation in helix 1a (125 Arg-Cys) was detected. The results of this study are consistent with previous reports and they demonstrate that the PASA method is a rapid and reproducible method for the detection of single-base changes and small deletions.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Mycopathologia 102 (1988), S. 129-133 
    ISSN: 1573-0832
    Keywords: asteroid body ; Sporothrix schenckii ; sporotrichosis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract A survey of 150 cases with sporotrichosis seen at the Dermatological Clinic of Kurume University Hospital from February 1962 to October 1986 was reported. The proportion of cases with sporotrichosis to the total number of outpatients was 0.17%. Greater percentage of cases fell into the less than 10 years old or more than 40 years old groups. The male to female ratio was 1∶1.46, and 38 cases occurred in farmers. Geographic distribution was remarkable, especially around the Chikugo and Yabe river. Sixty-four cases showed the cutaneous lymphangitic type and 85 cases the localized cutaneous type and one case atypical type. The face and upper extremities were the most affected. The sporotrichin test was positive in 117 of 131 cases. The causative organism was demonstrated in tissue sections in 69% of the cases.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 210 (1984), S. 639-646 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: S-100 protein, isolated from mammalian brain, has widely been used for immunohistochemical marker of the glia cells and the cells derived from the neural crest. In the present study, we made anti S-100 protein antibody and studied the immunoreactive distribution of S-100 protein in the cutaneous nervous system. Albino rabbits were immunized with S-100 protein and complete Freund adjuvant, and antiserum was purified by ion-exchange chromatography. Formalin-fixed normal human skin and sciatic nerve of rat were examined by the PAP method. S-100 protein was detected in Schwann cells of sciatic nerve of rat and cutaneous nerve bundles of human skin specimens. Meissner corpuscles and inner core cells of Pacinian corpuscles of human skin were S-100 protein positive. These findings suggest that the staining of S-100 protein with PAP method is a simple and reliable method to demonstrate the cutaneous nervous system. Also, lamellar cells of Meissner corpuscles and inner core cells of Pacinian corpuscles are indicated to be Schwann cell origin.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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