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Bibiana Prez M. Isabel Gmez Enrique Snchez Ernesto Muoz Antonio Ledo 《The Journal of dermatology》1995,22(1):43-45
Pachydermodactyly is an uncommon variant of digital fibromatosis that has previously been related to knuckle pads. It is a benign condition that needs no investigation for an underlying systemic disease. We present a new case of pachydermodactyly and comment on the available literature. 相似文献
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Alicia T. Dagrosa MD MBA Lindsey W. Fraser MD Konstantinos D. Linos MD Aravindhan Sriharan MD Daniel A. Albert MD Julianne A. Mann MD 《Pediatric dermatology》2020,37(5):907-910
Pachydermodactyly is an uncommon, progressive, nontender thickening of the fingers with prominent involvement of the proximal interphalangeal joints. Pachydermodactyly mimics inflammatory arthritis but plain film radiography is normal in this condition. Pachydermodactyly has been previously described in workers performing manual labor. Mechanical stimulation has been identified as a predisposing factor in the majority of cases. We present three cases in adolescent males arising in association with excessive computer gaming. 相似文献
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Pachydermodactyly in Two Young Girls 总被引:1,自引:0,他引:1
Federico Bardazzi M.D. Iria Neri M.D. Pier Alessandro Fanti M.D. Annalisa Patrizi M.D. 《Pediatric dermatology》1996,13(4):288-291
Abstract: Pachydermodactyly is a benign, superficial fibromatosis frequently observed in young males. We describe the condition in two young girls affected by Ehlers-Danlos syndrome (EDS) and tuberous sclerosis, respectively. We hypothesized that in the patient with tuberous sclerosis, pachydermodactyly is a clinical manifestation of the associated systemic disease, whereas obsessive-compulsive behavior is probably the main cause in the girl with EDS. 相似文献
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Pachydermodactyly (PDD) is a rare, benign form of digital fibromatosis and this is characterized by asymptomatic soft tissue swelling that affects the lateral aspects of the proximal interphalangeal (PIP) joints of the fingers. Although the etiology of PDD is unknown, the possibility of repetitive minor trauma by habitual or compulsive habits of interlacing the fingers or rubbing of the fingers has been suggested as a cause by several authors. We experienced a 14-year-old boy who was diagnosed as having PDD by the clinical manifestations and this was supported by a radiological study and the routine laboratory tests. He also had the habit of repetitively manipulating his hands when feeling emotional distress. PDD sometimes can be misdiagnosed as a rheumatic condition. Although an unusual disorder, PDD should be considered in the differential diagnosis of patients who present with digital bulbous swelling. 相似文献
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Vivian Balassiano Celso Tavares Sodré Marcia Ramos-e-Silva 《Journal of the European Academy of Dermatology and Venereology》1996,6(3):260-263
We report a case of pachydermodactyly, a rare entity characterized by acquired diffuse swelling of the lop and sides of the fingers. 相似文献
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Eosinophic fasciitis (EF) is an uncommon connective tissue disease characterized by scleroderma-like cutaneous changes, peripheral eosinophilia, hypergammaglobulinemia, and an elevated erythrocyte sedimentation rate (ESR). Typical histopathologic findings include chronic inflammatory infiltration affecting the deep fascia with lymphocytes, histiocytes, and occasionally eosinophils. We report two cases of EF, the first of which is a 36-year-old man with a tender brownish induration on both forearms, for 2 months. Histopathologic examination showed fibrotic fascia with a mixed inflammatory cell infiltration. The second case is a 52-year-old woman with a symmetrical painful swelling and skin induration on both forearms, for 4 months. A deep biopsy demonstrated chronic inflammatory cell infiltration and hyaline degeneration in the fascia. Increased signal intensity in the fascia and tendon sheath was shown on magnetic resonance imaging. In laboratory examination, mild eosinophilia was found in both cases. Both patients had a history of physical activity (weight training and excessive housework, respectively) and showed marked improvement with high doses of oral prednisolone for several months. 相似文献
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报告2例隆突性皮肤纤维肉瘤。例1男,37岁,左侧肩部红色斑块20年;例2女,64岁,左侧腹股沟包块7年。皮损组织病理均示真皮全层大量的梭形肿瘤细胞,排列成席纹状或漩涡状,部分肿瘤细胞核大、深染,部分核分裂。均诊断为:隆突性皮肤纤维肉瘤。 相似文献
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胎传梅毒2例 总被引:2,自引:0,他引:2
刘德润 《中国皮肤性病学杂志》2003,17(1):32-32
<正> 例1女,30天,顺产。因鼻塞、气急、咳嗽、发热20余天来就诊。生后1周出现鼻塞、流涕、口唇干裂,唇周红斑、痂皮,渐加重,咳嗽、发热,T37.5℃。外院诊断“上呼吸道感染”,给予“止咳糖浆、先锋霉素”治疗3天,症状稍缓解,体温降至正常。2周后面部皮疹加重,后背、臀、肛周、四肢出现红斑及小红丘疹,尤以口周、颈前、臀部皮疹为重,并出现水疱,在当地给予“炉甘石洗剂、扑尔敏”等药物治疗无效,遂来我科就诊。体检: 相似文献
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胎传梅毒2例 总被引:1,自引:0,他引:1
例 1,女 ,45天。生后 1月余双上下肢、手足见类圆形红斑及暗红斑 ,部分红斑上有少许脱屑 ,以双手足为甚 ,伴发热。WBC 12 .5× 10 9/L。TPHA(+ ) ,RPR 1∶3 2阳性 ,其母TPHA(+ ) ,RPR 1∶16阳性。例 2 ,男 ,7天。生后 2h出现双手足脱屑性、浸润性铜红色斑 ,见脓疱 ,渐蔓延至周身 ,伴发热 ,活动受限。一般状态欠佳 ,四肢呈软瘫状。WBC14 .0× 10 9/L ,RPR 1∶16阳性 ,TPHA(+ )。其父、母均TPHA(+ ) ,RPR 1∶16阳性。诊断 :胎传梅毒。予青霉素治疗 相似文献
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例1男,26岁,四肢间断皮疹8年;例2女,16岁,左上肢、双下肢皮疹15年,逐渐加重。皮疹为大理石样,肢端下垂后明显。 相似文献