摘要:

AbstractThe patient is an obese, 55‐year‐old woman. She noticed purpura at several sites when she was 49 years old. She visited our clinic with a chief complaint of exertional dyspnea at 51 years of age. Physical examination revealed localized edema in the left chest wall and lower abdomen with translucent papules in the center. Macroglossia, hemorrhagic macules, loss of axillar and pubic hairs, and goose‐egg sized swellings of submaxillar lymph nodes were also found. Laboratory data were within the normal range except an increase of IgD and low ECG voltage. Bone‐marrow puncture revealed an increase (27%) of plasma cells with some atypicality. Serum immunoelectrophoresis clarified IgD λ‐type paraproteinemia and λ‐type Bence Jones proteinemia.Histologically, edema with an increase in GAG was conspicuous in the circumscribed areas of the middle dermis. Amyloid deposition was clarified in the walls of arterioles in th

ISSN:0385-2407    

DOI:10.1111/j.1346-8138.1989.tb01221.x

年代:1989

数据来源: WILEY

摘要:

AbstractA 50‐year‐old man had a primary malignant melanoma of the penis associated with granuloma telangiectaticum in the pigmented lesion. The patient had an operation for phimosis at the age of 20 and after the operation, he noticed a pigmented lesion at the operation site.We examined the literature and found 16 cases of primary malignant melanoma of the penis in Ja

ISSN:0385-2407    

DOI:10.1111/j.1346-8138.1989.tb01222.x

年代:1989

数据来源: WILEY

摘要:

AbstractA 61‐year‐old Japanese man with chronic myelogenous leukemia developed pityriasis lichenoides‐like eruptions during chemotherapy. Histopathological features were also consistent with the disease.The eruption in this case may have been an allergic reaction arising in a depressed immunity induced by chemoth

ISSN:0385-2407    

DOI:10.1111/j.1346-8138.1989.tb01223.x

年代:1989

数据来源: WILEY

摘要:

AbstractA 70‐year‐old male forestation worker had a tick‐bite on the lower abdominal skin. The bite was treated by surgical excision of the tick together with the surrounding skin. The tick was identified asIxodes ovatusNeumann through investigation of its morphological characteristics. This patient is the fourth case of a tick‐bite fromIxodes ovatusNeumann in wester

ISSN:0385-2407    

DOI:10.1111/j.1346-8138.1989.tb01224.x

年代:1989

数据来源: WILEY

摘要:

AbstractA case of a 70‐year‐old man with several dome‐shaped tumors with acantholysis was reported. The histopathological findings of these black‐brownish colored tumors on the back were compatible with seborrheic keratosis, consisting of basaloid and squamoid cells.Although three cases reported by Tagami et al. (1978) and Uchiyama et al. (1986) showed intraepidermal epithelioma‐like tumor nests in the acanthotic lesions, our case was thought to correspond to another variant of seborrheic keratosis with aca

ISSN:0385-2407    

DOI:10.1111/j.1346-8138.1989.tb01225.x

年代:1989

数据来源: WILEY

摘要:

AbstractA 36‐year‐old female patient with scleroderma/Sjögren's syndrome developed multiple cystic tumors on the dorsal aspect of her left hand, right elbow, and left shoulder joint two years after the onset of scleroderma. Histologically, amorphous eosinophilic substances located in subcutaneous tissue showed a strong positive reaction to PTAH and rosindole stain, and focal positive reaction to Von Kossa stain. Rheumatoid rice body like substances with chalky fluid were discharged from tumoral lesions. From these results, this case was diagnosed as tumoral calcinosis secondary to connective tissue degeneration due to the pathogenetic mechanism underlying scleroderma/Sjögren's syn

ISSN:0385-2407    

DOI:10.1111/j.1346-8138.1989.tb01226.x

年代:1989

数据来源: WILEY

ISSN:0385-2407    

DOI:10.1111/j.1346-8138.1989.tb01227.x

年代:1989

数据来源: WILEY