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https://www.readbyqxmd.com/read/29915775/severe-hypertriglyceridemia-presenting-as-eruptive-xanthomatosis
#1
Sameera S Vangara, Kyle D Klingbeil, Raymond M Fertig, Jason L Radick
Eruptive xanthomatosis is described as the sudden eruption of erythematous yellow papules in the presence of hypertriglyceridemia, often associated with serum triglyceride levels above 2000 mg/dl. Severe hypertriglyceridemia can be caused by primary genetic mutations, secondary chronic diseases, or a combination of both. Uncontrolled diabetes mellitus is a known risk factor. It is imperative for physicians to be aware of eruptive xanthomatosis as a warning sign for severe hypertriglyceridemia due to the underlying risk for the potentially fatal complication of acute pancreatitis...
January 2018: Journal of Family Medicine and Primary Care
https://www.readbyqxmd.com/read/29914897/concurrent-metastases-of-papillary-thyroid-carcinoma-to-the-scalp-and-meckel-s-cave
#2
Patrick S Phelan, Jamie L Mull, Mohamed Z Rajput, Amy C Musiek
We present the case of a 65-year-old man with severe headaches and unilateral facial weakness, seen in consultation by the dermatology service to rule out primary cutaneous melanoma after brain imaging identified an enlarging mass within the right trigeminal (Meckel's) cave. Examination revealed only a pair of erythematous papules on the scalp, for which biopsy demonstrated metastatic papillary thyroid carcinoma. Further evaluation and subsequent thyroidectomy confirmed the origin of widespread internal disease, followed by definitive excision of scalp lesions and multimodal management of systemic involvement...
June 17, 2018: BMJ Case Reports
https://www.readbyqxmd.com/read/29911526/the-prevalence-of-malassezia-folliculitis-in-patients-with-papulopustular-comedonal-acne-and-their-response-to-antifungal-treatment
#3
Seda Pürnak, Murat Durdu, Mustafa Agah Tekindal, A Tülin Güleç, Deniz Seçkin
Because Malassezia folliculitis (MF) may clinically mimic acne vulgaris (AV), patients usually receive unnecessary and prolonged antibiotic treatment. We aimed to determine the prevalence of MF among patients with AV, and to evaluate its response to antifungal treatment. A total of 217 patients with AV underwent cytologic examination for the presence of Malassezia yeasts. Samples were obtained from lesional and nonlesional skin and stained with May-Grünwald-Giemsa. MF was diagnosed if there were more than six spores in one microscopic field (at ×400 magnification)...
2018: Skinmed
https://www.readbyqxmd.com/read/29904308/histiocytoid-sweet-syndrome-successfully-treated-with-etanercept
#4
Ian T Watson, Isabel Haugh, Alexis R Gardner, M Alan Menter
We report the first case of a 34-year-old woman with histiocytoid Sweet syndrome (HSS) that was successfully treated with etanercept. HSS is a rare histological variant of acute febrile neutrophilic dermatosis that was described by Requena et al in 2005. It is distinguished by dermal infiltration by mononuclear cells with a histiocytic morphology. To date there are three reported cases of the use of etanercept in the treatment of classic febrile neutrophilic dermatosis but none targeting this disease variant...
July 2018: Proceedings of the Baylor University Medical Center
https://www.readbyqxmd.com/read/29894529/squamoid-eccrine-ductal-carcinoma
#5
Jason Jacob, Lisa Kugelman
Squamoid eccrine ductal carcinoma (SEDC) is an extremely rare cutaneous tumor of unknown etiology. We report the case of a 77-year-old man with a history of treated chronic lymphocytic leukemia along with numerous basal cell and squamous cell carcinomas who presented for evaluation of a 5-cm, stellate, sclerotic plaque on the left chest of approximately 2 years' duration and a suspicious 3-mm pink papule on the right nasal sidewall of 2 months' duration. Initial histology of both lesions revealed carcinoma with squamous and ductal differentiation that extended from the undersurface of the epidermis, favoring a diagnosis of SEDC...
May 2018: Cutis; Cutaneous Medicine for the Practitioner
https://www.readbyqxmd.com/read/29888407/epidemiology-of-kaposi-sarcoma-review-and-description-of-the-nonepidemic-variant
#6
REVIEW
Ramya Vangipuram, Stephen K Tyring
Kaposi sarcoma (KS) is a rare angioproliferative tumor whose etiology is associated with human herpesvirus 8 (HHV 8). KS lesions typically involve the skin or mucosal surfaces and are characterized by purplish, red-blue, or brown-black macules, papules, and nodules which are prone to bleeding and ulceration. Definitive diagnosis requires biopsy revealing characteristic angioproliferative features. There are four widely recognized types of KS, which are histologically indistinguishable but differ in epidemiology and prognosis...
June 11, 2018: International Journal of Dermatology
https://www.readbyqxmd.com/read/29888012/two-cases-of-delayed-diagnosis-of-leprosy-in-mauritania
#7
Boushab Mohamed Boushab, Fatima-Zahra Fall-Malick, Leonardo K Basco
Leprosy is a chronic infectious disease that mainly affects the skin, mucous membranes, and peripheral nervous system. The clinical manifestations of leprosy are numerous and polymorphic with the most frequent signs involving skin and neurological damage. Some of its manifestations, such as joint pain, are unusual. Its elimination as a public health problem in many countries seems to lead to a lack of practical knowledge among health care personnel and as a consequence a risk of late diagnosis. As in other countries, leprosy has become rare in Mauritania...
2018: Case Reports in Dermatological Medicine
https://www.readbyqxmd.com/read/29883338/-gout-or-squamous-cell-cancer-of-the-ear-in-a-91-year-old-man-diagnostic-and-therapeutic-problems-a-case-report
#8
Andrzej N Majda, Aleksandra Majdan, Paweł Piłat, Paweł Cisek
Gout tophi around auricular area are common in old men. The differential diagnosis of papules or nodules on the ear includes tophaceous gout, rheumatoid nodules, basal or squamous cell cancer, melanoma, verruca vulgaris or actinic keratosis. The presence of the skin cancer, most commonly located on the head and neck, is often related to the long exposure of the skin to sunlight. Elderly patients are the predominant group of patients with skin malignancies. The aim of this study is to emphasize the importance of early cancer detection in elderly people and use of appropriate therapeutic options that take into account the special requirements of geriatric patients...
2018: Wiadomości Lekarskie: Organ Polskiego Towarzystwa Lekarskiego
https://www.readbyqxmd.com/read/29881579/gout-tophi-on-the-soles-resembling-viral-warts
#9
Simon Bossart, Daniel Sidler, Roland Blum, Robert E Hunger
This case highlights the need to consider tophaceous gout in patients with post-transplant renal insufficiency, chronic immunosuppression, and hypertension, who develop atypical papules or nodules on the soles, which can cause problems in differentiation from other skin diseases.
June 2018: Clinical Case Reports
https://www.readbyqxmd.com/read/29877895/self-healing-cutaneous-mucinosis-in-adulthood-the-adult-counterpart-of-the-juvenile-variant-of-the-disease
#10
Gustavo Deza, Pablo García-Martínez, Fernando Gallardo, Carlos Barranco, Ramon M Pujol
Self-healing cutaneous mucinosis (SHCM) is an idiopathic localized cutaneous mucinosis mainly described in children and characterized clinically by an acute onset of papules and nodules that exhibit a spontaneous resolution in a period ranging from weeks to few months. Histologically, a diffuse mucin deposition in the dermis and/or hypodermis associated with a proliferation of spindle-shaped cells and some large epithelioid gangliocyte-like mononuclear cells is usually observed. An uncommon adult variant of SHCM has also been reported; however, the clinicopathological features described in these patients are extremely heterogeneous and differ significantly from the juvenile variant of the disease, often showing exclusively dermal involvement...
June 1, 2018: American Journal of Dermatopathology
https://www.readbyqxmd.com/read/29867429/successful-treatment-of-pityriasis-rubra-pilaris-with-ixekizumab
#11
Kathrin Hanfstingl, Agnes Pekar-Lukacs, Reinhard Motz, Emmanuella Guenova, Wolfram Hoetzenecker
Pityriasis rubra pilaris is an inflammatory dermatologic disorder of unknown cause and often confounded with psoriasis. It is characterised by hyperkeratotic follicular papules, scaly erythematous plaques, palmoplantar keratoderma, and a progression to generalised erythroderma. Here, we report the case of a 68-year-old man with pityriasis rubra pilaris, who was successfully treated with ixekizumab, an interleukin-17A inhibitor.
May 2018: Case Reports in Dermatology
https://www.readbyqxmd.com/read/29851124/acneiform-follicular-mucinosis-an-indolent-follicular-mucinosis-variant-unrelated-to-mycosis-fungoides
#12
S Geller, M Pulitzer, P L Myskowski
Follicular mucinosis (FM) can present as an acneiform eruption, and is usually a benign variant of primary FM unrelated to cutaneous T-cell lymphoma (CTCL). We report two cases of women in their twenties who presented with an acneiform rash on the face, arms and back. In both cases, pathological evaluation of the facial papules revealed predominantly mucinous degeneration of the follicular epithelium, with insufficient lymphocytic infiltration or atypia to diagnose mycosis fungoides. These cases are similar to previous reports of acneiform FM...
May 30, 2018: Clinical and Experimental Dermatology
https://www.readbyqxmd.com/read/29848519/subcutaneous-oedema-of-upper-limbs-heralding-an-aggressive-form-of-dermatomyositis
#13
Mohit Shukla, Rishi Patel, Halyna Kuzyshyn, David Feinstein
Subcutaneous oedema is a rare presenting clinical manifestation of dermatomyositis. In this case, we report a 44-year-old man presenting with bilateral upper extremity predominant swelling and weakness. The proximal muscle weakness, dysphagia and presence of Gottron's papules as well poikiloderma like skin changes led to the clinical diagnosis of dermatomyositis. He received aggressive treatment with high-dose glucocorticoids and required intravenous immunoglobulin with improvement in his symptoms.
May 30, 2018: BMJ Case Reports
https://www.readbyqxmd.com/read/29845945/answer-to-photo-quiz-asymptomatic-facial-papules-as-a-marker-of-genetic-syndrome
#14
(no author information available yet)
No abstract text is available yet for this article.
May 2018: Netherlands Journal of Medicine
https://www.readbyqxmd.com/read/29845944/asymptomatic-facial-papules-as-a-marker-of-genetic-syndrome
#15
A Calleja Algarra, V Velasco Tamariz, R Aragón Miguel, M Prieto Barrios, B Pinilla Martín, R Llamas Martín, P L Ortiz Romero, V Monsálvez Honrubia
No abstract text is available yet for this article.
May 2018: Netherlands Journal of Medicine
https://www.readbyqxmd.com/read/29845618/solvent-orange-60-is-a-potent-contact-sensitizer-in-occupational-and-everyday-life
#16
Kotryna Linauskienė, Erik Zimerson, Annarita Antelmi, Magnus Bruze, Lina Hagvall, Nils Hamnerius, Inese Hauksson, Kristina Ryberg, Marléne Isaksson
BACKGROUND: Solvent Orange (SO) 60 is a perinone-type dye that is often used in plastic materials such as spectacle frames and has been shown to cause contact allergy. The first case of SO 60 allergic contact dermatitis caused by spectacle frames was reported in 1999, and the second in 2011. We have recently seen 10 patients, of whom 6 developed dermatitis in the retroauricular/temporal area after wearing plastic spectacles. OBJECTIVES: To report the cause of the dermatitis in the 10 patients and to describe our first case with occupational SO 60 contact allergy...
May 30, 2018: Contact Dermatitis
https://www.readbyqxmd.com/read/29806684/-trichodysplasia-spinulosa-report-of-one-case
#17
Cristián Navarrete-Dechent, Carolina Cevallos, Juan Jorge Manríquez, Claudio Salazar, Sergio González
Trichodysplasia spinulosa is a rare disease that occurs in the setting of immunosuppression, associated with tolerogenic therapy used in allograft recipients or patients with hematologic malignancies. Clinically, it is characterized by a centrofacial cutaneous eruption of erythematous papules with a central keratinous spicule, often associated with variable degrees of alopecia. Histologic findings are characteristic, and electron microscopy reveals the presence of trichodysplasia spinulosa associated polyomavirus...
January 2018: Revista Médica de Chile
https://www.readbyqxmd.com/read/29805815/granuloma-annulare-in-the-setting-of-secukinumab
#18
Matthew L Clark, Courtney A Tobin, Angela Sutton, Tricia Ann Missall
Granuloma annulare (GA) is a common benign inflammatory skin condition classically presenting as skin-colored to erythematous dermal papules and annular plaques. Histologically, GA displays a dermal granulomatous infiltrate with palisaded histiocytes surrounding focally altered collagen. The exactly etiology of GA remains unknown, but it has been associated with trauma, various infections, diabetes mellitus, malignancy, thyroid disease, dyslipidemia, and several medications. In 2017, a case of GA developing in a patient treated with the interleukin 17A antagonist secukinumab was reported...
2018: Case Reports in Dermatological Medicine
https://www.readbyqxmd.com/read/29800987/firm-papules-and-nodules-on-face-neck-and-thorax
#19
Zhong-Shuai Wang, Jun Li
No abstract text is available yet for this article.
May 9, 2018: JAMA Dermatology
https://www.readbyqxmd.com/read/29797732/eruptive-poromatosis-in-a-patient-with-breast-cancer
#20
T M Lim, J Weir, L Fearfield
Poromas are a group of benign growths of poroid differentiation derived from cells of the terminal duct and connected to the epidermis, normally presenting as solitary papules, plaques or nodules. Rarely they can be eruptive in nature and as such are described as poromatosis. We report an unusual case of widespread poromatosis occurring in a woman with metastatic breast cancer who had recently completed chemo-radiotherapy. This article is protected by copyright. All rights reserved.
May 24, 2018: Journal of Cutaneous Pathology
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