Skin changes

  • 文章类型: Case Reports
    骨软骨瘤是最常见的骨良性肿瘤,可以是无柄的或有蒂的。虽然骨软骨瘤通常见于长骨,它们很少在手或脚的小骨头中看到。寻常疣,也被称为普通疣,是医生最常见的皮肤疾病之一,必须在临床或组织学上与其他过度角化疾病区分开来,包括骨骼疾病,如骨肿瘤,可以对皮肤施加压力,并导致骨痂形成,可以模仿疣或造成皮肤畸形。在评估患者的皮肤状况时,应考虑高度怀疑潜在的骨量或肿瘤。特别是手或脚,无法通过治疗改善。
    该病例报告介绍了一名20岁的男性,其左第四指骨远端有蒂骨软骨瘤,角化过度的皮肤覆盖脚趾末端的肿块。最初由家庭医生和足病医生治疗寻常疣超过5年,当治疗足病医生遇到骨骼和推荐的X光片时,他采用液氮冷冻疗法和手术切除肿块的两种治疗方法。几天后,家人被告知患者患有骨肿瘤后,要求对我们的实践进行随访。患者要求手术切除继发于疼痛的骨软骨瘤,其活动和作为飞行员的职业困难。
    所有医生都必须注意出现皮肤变化的患者的潜在骨肿瘤或肿块,尤其是脚或手。在评估和治疗患有皮肤病变的患者时,知道潜在的骨肿瘤可以表现为寻常疣,可以防止诊断延迟或不必要的治疗。幸运的是,我们的病例是良性骨软骨瘤;恶性肿瘤延迟诊断可能导致肢体或生命丧失.
    UNASSIGNED: Osteochondromas are the most common benign tumors of the bone and can be sessile or pedunculated. Although osteochondromas are typically seen in the long bones, they are rarely seen in the small bones of the hand or foot. Verruca vulgaris, also known as the common wart, is one of the most common skin conditions presenting to physicians and must be distinguished either clinically or histologically from other hyperkeratotic conditions, including bone conditions such as bone tumors that can place pressure on the skin and cause callus formation that can mimic a wart or create skin deformity. A high index of suspicion for underlying bone mass or tumor should be entertained when evaluating patients for skin conditions, particularly of the hand or foot, with failure to improve with treatment.
    UNASSIGNED: This case report presents a 20-year-old male with a pedunculated osteochondroma of the left fourth distal phalanx with hyperkeratotic skin overlying the mass at the end of the toe. He was initially treated by a family doctor and podiatrist for verruca vulgaris for over 5 years with two treatments of liquid nitrogen cryotherapy and surgical excision of the mass when the treating podiatrist encountered bone and recommended radiographs. The family requested follow-up with our practice several days later after they were told the patient had a bone tumor. The patient requested surgical excision of the osteochondroma secondary to pain with activities and difficulties with his vocation as a pilot.
    UNASSIGNED: All physicians must be mindful of an underlying bone tumor or mass in patients presenting with skin changes, particularly about the foot or hand. Knowledge that an underlying bone tumor can present as a verruca vulgaris may prevent a delay in diagnosis or unnecessary treatment when evaluating and treating a patient with a skin lesion. Fortunately, our case was a benign osteochondroma; a malignant tumor with a delay in diagnosis could lead to loss of limb or life.
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  • 文章类型: Case Reports
    多发性神经病,器官肿大,内分泌病,单克隆浆细胞疾病,和皮肤变化(POEMS)综合征是一种多系统疾病,治疗选择有限。这里,我们描述了一个55岁的女性受试者接受多种药物治疗的病例,但皮肤症状持续进展;患者对baricitinib反应良好.这表明JAK/STAT信号通路在POEMS综合征的病理过程中起着至关重要的作用。
    Polyneuropathy, organomegaly, endocrinopathy, monoclonal plasma cell disorder, and skin changes (POEMS) syndrome is a multisystem disorder that has limited treatment options. Here, we described a case of a 55-year-old female subject who was treated for multiple drugs, but the skin symptoms continued to progress; the patient responded well to baricitinib. This suggests that JAK/STAT signaling pathways play an essential role in the pathological process of POEMS syndrome.
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  • 文章类型: Case Reports
    多发性神经病,器官肿大,内分泌病,单克隆浆细胞疾病,皮肤改变(POEMS)综合征是一种与潜在的浆细胞肿瘤相关的多系统疾病。这里,我们介绍了两例POEMS综合征,在磁共振神经造影上表现为骨量增加并伴有皮质破坏,直接侵入神经根和腰臀肌。以前没有报道过这些特征。我们还报告了一例弥漫性肥大和臂丛和腰骶丛增强的病例,模拟最常见的慢性炎性脱髓鞘性多发性神经根神经病。此外,我们在神经丛中发现了神经鞘积液,再加上各种肌筋膜炎和失神经肌肉萎缩。该病例系列关注骨骼和周围神经系统中POEMS综合征的非典型磁共振成像发现,作为关键的攻击靶器官,这将有助于诊断。
    Polyneuropathy, organomegaly, endocrinopathy, monoclonal plasma cell disorder, skin changes (POEMS) syndrome is a multisystem disease associated with underlying plasma cell neoplasm. Here, we present two cases of POEMS syndrome that manifested on magnetic resonance neurography as an increasing bone mass with cortical disruption, direct invading nerve roots and lumbar gluteal muscles. These features have not been previously reported. We also report a case with diffuse hypertrophy and enhancement of the brachial and lumbosacral plexus, which mimics the most common chronic inflammatory demyelinating polyradiculoneuropathy. Moreover, we detected perineurium effusions in the plexus, coupled with a variety of myofascitis and atrophy in denervated muscle. The case series is of concern to atypical magnetic resonance imaging findings of POEMS syndrome in the bone and peripheral nerve system as critical attacked target organs, which would be facilitating diagnosis.
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  • 文章类型: Case Reports
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  • 文章类型: Journal Article
    A histological evaluation of peeling-induced skin changes in subcutaneous undermined preauricular facial skin flaps of nine patients was performed. There were three treatment groups: Trichloroacetic acid (TCA) 25%, TCA 40% and phenol/croton oil; one group served as control. Two independent evaluators determined the epidermal and dermal thickness and the depth of necrosis (micrometre). The percentual tissue damage due to the peeling was calculated, and a one-sample t-test for statistical significance was performed. On the basis of the histomorphological changes, peeling depth was classified as superficial, superficial-partial, deep-partial and full thickness chemical burn. The histological results revealed a progression of wound depth for different peeling agents without full thickness necrosis. TCA peels of up to 40% can be safely applied on subcutaneous undermined facial skin flaps without impairing the vascular patency, producing a predictable chemical burn, whereas deep peels such as phenol/croton oil peels should not be applied on subcutaneous undermined skin so as to not produce skin slough or necrosis by impairing vascular patency.
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  • 文章类型: Case Reports
    The authors report a case of sensorimotor polyneuropathy, diffuse cutaneous hyperpigmentation, skin sclerodermiform thickening and papular lesions in the infraclavicular and abdominal region. Besides weight loss, there were diabetes mellitus and hypothyroidism. The alterations were consistent with POEMS (Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal gammopathy and Skin changes) syndrome, which is a rare systemic disease with monoclonal proliferation of plasmacytes and slow progression. Cutaneous alterations are present in 68% of patients with diffuse cutaneous hyperpigmentation, plethora and acrocyanosis. Leukonychia, necrotizing vasculitis, hypertrichosis and cutaneous thickening of sclerodermiform type are also cited. The onset of multiple cutaneous angiomas in this syndrome has been observed in 24-44% of patients.
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