Yellowish slightly elevated plaques on the patient’s left cheek. 

Yellowish slightly elevated plaques on the patient’s left cheek. 

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We report on a 70-year-old woman with diffuse normolipemic plane xanthoma (DNPX) who developed macular yellowish patches on the eyelids, both cheeks, and the nose. Histology revealed the accumulation of CD68-positive foam cells and Touton giant cells in the superficial dermis. Plasma lipid levels were within normal limits. The patient had no underl...

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... normolipemic plane xanthoma (DNPX) was first described by Altman and Winkelmann in 1962 [1]. The features of this entity are: (1) xanthelasma palpebrarum; (2) diffuse xanthoma planum of the head, neck, trunk, and extremities, and (3) plasma lipid values that are within normal limits. Several associations have been reported between DNPX and lymphoproliferative and myeloproliferative disorders, particularly multiple myeloma and benign monoclonal gammopathy (often IgA) [2, 3]. All therapeutic options for the treatment of plane xanthoma include mechanical removal by excision, chemabrasion, dermabrasion, or abrasive laser therapy [4 – 6]. We report on a patient with DNPX who received oral probucol and showed significant clearing of the lesions. We suggest that probucol be included as a primary therapy for DNPX. A 70-year-old woman presented with well-defined macular yellowish patches on her eyelids, both cheeks, and the nose lasting over a few years (fig. 1). She had no history of topical steroid use or extensive sun exposure on her face. Her medical history was unre- markable. A skin biopsy specimen revealed the accumulation of foam cells and Touton giant cells in the superficial dermis (fig. 2). These cells were CD68 positive, and CD1a and S-100 negative. Complete blood count, and liver and renal function tests were within normal limits, but she had elevated levels of IgA [460.7 mg/dl (normal values: 100 – 400 mg/dl)] and amylase [270 IU/l (normal values: 40 – 120 IU/l)]. No M protein was noted. Plasma lipid levels including total cholesterol, HDL and LDL cholesterols, triglycerides, and apolipopro- teins were normal. Chest X-ray and abdominal ultrasonography were also normal. She was diagnosed with idiopathic macroamylasemia and treatment was considered unnecessary. Based on the clinical and histopathological findings, a diagnosis of DNPX was made and oral administration of probucol (500 mg/day) was initiated. The lesions began to recede after 2 weeks and had almost resolved within 8 months (fig. 3). DNPX, first described in 1962 [1], is characterized by diffuse, yellow to orange, slightly elevated plaques with sharply delineated borders that may affect any part of the body. Normolipemic cutaneous xanthoma can be categorized into 3 groups: type I – III. Type I contains patients with xanthomas found in association with an altered lipoprotein content or structure. Type II is associated with an underlying lymphoproliferative disease. Type III consists of patients with neither lipoprotein abnormalities nor underlying systemic disease, but in whom local tissue alterations seem to play a role in xanthoma formation [7]. Several therapeutic options exist for the treatment of plane xanthoma. Lesions can be removed by excision, chemabrasion, dermabrasion, or abrasive laser therapy [4 – 6]. Lorenz et al. [4] used an Er:YAG laser for full-face DNPX lesions under general anesthesia and reported that the lesions were almost completely removed after 2 sessions. Although these excisional or abrasive therapies may be useful for limited lesions including palpebral xanthelasmas, they may be too invasive for widespread lesions. In addition, a risk of scarring has been associated with these treatments. Therefore, another therapeutic option with medication may be warranted. Probucol is an antioxidant that may inhibit atherogenesis by limiting the oxidative modification of LDL cholesterol [8, 9] and, thus, foam cell formation and/or endothelial cell injury [9]. It has been used for the treatment of hypercholesterolemia in some countries including Japan [8]. Harris et al. [10] showed that xanthelasma lesions decreased in size in their 7 cases, and 3 lesions disappeared during probucol therapy in patients with hypercholesterolemia. Furthermore, 17 out of 25 xanthelasma patients (68%) with normolipemia exhibited regression after taking probucol [11]. Therefore, we used probucol to treat our patient with DNPX. The results obtained were remarkable, and we suggest that probucol be included as a primary therapy for ...

Citations

... They are not a disease but rather symptoms of various lipoprotein problems or occur without an underlying metabolic defect [2] . statisfactory medical management of xanthelasma [9][10][11] . Isolated xanthelasma palpebrarum may be cauterised or excised if not associated with any systematic disturbances. ...
... 1,4 For diffuse plane xanthomas, there are rare case reports of treatments with erbium:YAG laser, 7 topical simvastatin 8 and systemic probucol. 9 We describe a rare case of lipoproteinemia X with complete resolution of xanthomas and normalization of the lipid panel after 18 weeks of conventional apheresis, even without a specific LDL filter. ...
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Cutaneous xanthomas are the result of dermal deposition of lipid, mostly caused by disorders of lipid metabolism. Less commonly, they occur in the setting of cholestatic liver disease, leading to accumulation of lipoprotein X, a rare form of dyslipidemia that does not respond well to conventional treatments. We describe an atypical presentation of sudden diffuse xanthomas secondary to lipoprotein X dyslipidemia in the context of cholestatic fulminant hepatitis caused by trimethoprim-sulfamethoxazole hypersensitivity. Histopathology was also atypical and showed an unusual verrucous appearance consisting of overlying epidermal hyperplasia with hyperkeratosis. Our patient had significant improvement, after normalization of her lipid panel under cholestyramine and 13 sessions of apheresis, with topical corticosteroids offering some relief. This rare case shows the importance of recognizing atypical presentations of xanthomas, particularly when they do not respond to conventional dyslipidemia treatments.
... A confounding factor to our final diagnosis was its differential diagnosis with diffuse normolipemic plane xanthoma (DNPX). DNPX was first described by Altman and Winkelmann in 1962, and the features of this entity are: (a) xanthelasma palpebrarum, (b) diffuse plane xanthomas of the head, neck, trunk, or extremities, and (c) plasma lipid values that are within normal limits 7,8 . Its skin biopsy shows an accumulation of foam cells and Touton giant cells, along the infiltrated histiocytes that are CD68 positive, and CD1a and S-100 negative. ...
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Symmetrical giant facial plaque-type juvenile xanthogranuloma (SGFP-JXG) is a rare variant of juvenile xanthogranuloma, reported only in two cases in the literature. We report a case of a 3-year-old Korean boy who developed bilateral yellowish indurated plaques on both cheeks since 1 year after birth. A skin biopsy revealed numerous foam cells and Touton type giant cells throughout the upper dermis, and its immunohistochemical studies resulted positive for CD68 and negative for S-100. The boy was therefore diagnosed as a persistent SGFP-JXG. As the lesion did not show any signs of spontaneous regression, we performed a single session of fractional ablative CO2 laser, which resulted in a significant reduction of the lesion. This is the first case report of a persistent SGFP-JXG on which a single ablative laser therapy was performed with a successful outcome.
... It is proposed that probucol, an antioxidant, acts by potentially inhibiting atherogenesis through limiting the oxidative modification of LDL cholesterol essential for foam-cell formation. [15] Miyagawa et al. [16] reported a case, of diffuse normolipemic plane xanthoma including XP, who was successfully treated with probucol. Harris et al. [17] showed 68% of xanthelasma regressed after probucol therapy. ...
... Probucol Case report [16] 1 Alirocumab ...
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Xanthelasmas are localized accumulation of lipid deposits on the eyelids. Lesions are typically asymptomatic and treatment is often sought for cosmetic purposes. Unfortunately, there is paucity of strong evidence in the literature for the effective treatment of normolipidemic xanthelasmas. A literature search using the term “xanthelasma” was carried out in PubMed and Medline databases. Only articles related to treatment were considered and analyzed for their data. Commonly cited treatments include topical trichloroacetic acid, liquid nitrogen cryotherapy, and various lasers including carbon dioxide, Er:YAG, Q-switched Nd:YAG, and pulse dye laser. However, traditional surgical excision has also been used. This article reviews these currently accepted modalities of treatment.
... However, many of these patients subsequently developed paraproteinaemia or dysglobulinaemia. 1 In addition to MGUS, multiple myeloma, leukaemia, adult T-cell lymphoma, cryoglobulinaemia, rheumatoid arthritis, Takayasu's arteritis and eosinophilic granulomatosis have all been described as being associated with the condition. 1,2 The skin lesions may precede the haematological or systemic disorder by many years. The cause of the xanthomatous deposition within the skin is not well understood, but a number of theories have been proposed. ...
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Article
Diffuse plane xanthomas (DPX) is a rare, chronic, metabolic skin disease which can seriously affect the appearance of the patients and result in psychological problems. Existing treatments are seriously limited. Our objective was to assess the efficacy of and tolerance to simvastatin ointment for the treatment of skin lesions in seven DPX patients. In this study, patients were treated twice daily on the right side of the lesions for 10 months with the 1% or 5% simvastatin ointment. Meanwhile, the left body was untreated as a contralateral controlled side. Efficacy was assessed via the change of rash and was further confirmed by histological study. For all seven participants, both the 1% and 5% simvastatin ointments were effective. The histological change in DPX showed significant decrease of foam cells in skin lesions. The immunohistochemical staining of CD68, macrophage scavenger receptor type 1, oxidized low‐density lipoprotein receptor 1 and Oil Red O became obviously reduced after treatment. The test medicines were safe with only some skin‐related side‐effects. This is the first research reported on simvastatin ointment treatment in DPX. Our results are the first to suggest that simvastatin ointment is effective in improving skin lesions of DPX clinically and histopathologically.
Chapter
This chapter will focus on the pharmacologic interventions for treatment of dyslipidemia in patients with chronic kidney disease (CKD). Herein, we will discuss drugs of interest for lipid management and their current and potential future use in CKD patients.
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Although metabolic diseases manifesting with cutaneous findings are rarely seen in daily practice, they emerge clinical significance as they can be the first manifestation of the systemic disease or can be seen in conjunction with other disorders. Among these diseases, scleromyxedema, diffuse normolipemic plane xanthoma, necrobiotic xanthogranuloma, amyloidosis and porphyria cutanea tarda can accompany myeloproliferative and lymphoproliferative diseases, as well as the malignancies of the solid organs. This paraneoplastic relationship can be diagnosed simultaneously at the time of the diagnosis of the cutaneous disease, or the cutaneous disease can precede the malignancy by several years. The recognition of these cutaneous diseases, appropriate screenings for the associated malignancies and the long term follow up of the patients can help to reduce the morbidity and mortality. Furthermore the treatment of the cutaneous disease can solely be possible with the management of the associated neoplasm.