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https://www.readbyqxmd.com/read/29457251/involvement-of-flexures-in-an-adolescent-patient-with-dermatomyositis-extension-of-inverse-gottron-papules
#1
A Bishnoi, D Parsad, U N Saikia
No abstract text is available yet for this article.
February 19, 2018: Clinical and Experimental Dermatology
https://www.readbyqxmd.com/read/29457012/impact-of-folliculitis-decalvans-on-quality-of-life-and-subjective-perception-of-disease
#2
Cristina Pindado-Ortega, David Saceda-Corralo, Laura Miguel-Gómez, Diego Buendía-Castaño, Pablo Fernández-González, Oscar M Moreno-Arrones, Pablo Fonda-Pascual, Adrian Alegre-Sánchez, Rita Rodrigues-Barata, Sergio Vañó-Galván
Folliculitis decalvans (FD) is a primary neutrophilic scarring alopecia characterized by perifollicular papules, crusts, and pustules frequently located on the vertex. FD may affect young men and women. Since it may lead to hair loss, it can have a negative impact on patients' quality of life. Nevertheless, studies have focused on clinical, prognostic, and therapeutic aspects without considering the psychological impact of FD. In our study, we found that FD patients experienced a considerable impact on their quality of life...
January 2018: Skin Appendage Disorders
https://www.readbyqxmd.com/read/29456618/an-unusual-presentation-of-adult-t-cell-leukemia-lymphoma
#3
Mohammed Tag-Adeen, Keiichi Hashiguchi, Yuko Akazawa, Ken Ohnita, Sawayama Yasushi, Niino Daisuke, Kazuhiko Nakao
Adult T-cell Leukemia/Lymphoma (ATL) is a rare disease, related to human T-lymphotropic virus-1 (HTLV-1) and presented mainly in adulthood by generalised lymphadenopathy, hepatosplenomegaly, skin lesions and hypercalcaemia, with rare gastrointestinal and/or oral manifestations. We reported this case to raise awareness and demonstrate the therapeutic challenges of this rare disease. A 49-year-old Japanese female presented with skin papules on both forearms, painful mouth ulcers and multiple neck swellings since early February 2017...
2018: Ecancermedicalscience
https://www.readbyqxmd.com/read/29450887/linear-yellow-papules-following-a-cat-scratch
#4
Julia S Lehman, Ashley M Nault, Steven A Smith, Marian T McEvoy
No abstract text is available yet for this article.
February 16, 2018: International Journal of Dermatology
https://www.readbyqxmd.com/read/29450880/a-review-of-cutaneous-manifestations-within-glucagonoma-syndrome-necrolytic-migratory-erythema
#5
REVIEW
Starling Tolliver, Jaqueline Graham, Benjamin H Kaffenberger
Necrolytic migratory erythema (NME) is a rare skin disorder that is a cutaneous manifestation of the glucagonoma syndrome. It presents with annular eruptions of migrating erythematous papules and plaques with superficial epidermal necrosis, central flaccid bullae, and crusted erosions located primarily in the intertriginous areas. Treatment with the long-acting somatostatin analog Octreotide is a potential therapy to help ameliorate skin symptoms. We present a case of a patient with a 1-year history of a pancreatic glucagonoma that developed an ulcerated, plaque-like, weeping rash over multiple areas of their body despite current treatment with Octreotide and stable pancreatic tumor staging...
February 16, 2018: International Journal of Dermatology
https://www.readbyqxmd.com/read/29450466/diagnostic-criteria-of-ulcerative-pyoderma-gangrenosum-a-delphi-consensus-of-international-experts
#6
Emanual Maverakis, Chelsea Ma, Kanade Shinkai, David Fiorentino, Jeffrey P Callen, Uwe Wollina, Angelo Valerio Marzano, Daniel Wallach, Kyoungmi Kim, Courtney Schadt, Anthony Ormerod, Maxwell A Fung, Andrea Steel, Forum Patel, Rosie Qin, Fiona Craig, Hywel C Williams, Frank Powell, Alexander Merleev, Michelle Y Cheng
Importance: Pyoderma gangrenosum is a rare inflammatory skin condition that is difficult to diagnose. Currently, it is a "diagnosis of exclusion," a definition not compatible with clinical decision making or inclusion for clinical trials. Objective: To propose and validate diagnostic criteria for ulcerative pyoderma gangrenosum. Evidence Review: Diagnostic criteria were created following a Delphi consensus exercise using the RAND/UCLA Appropriateness Method...
February 14, 2018: JAMA Dermatology
https://www.readbyqxmd.com/read/29447658/primary-anetoderma-with-undifferentiated-connective-tissue-disease
#7
Lana X Tong, Jenna Beasley, Shane Meehan, Evan Rieder, Miriam Pomeranz, Kristen Lo Sicco, Alisa Femia, Randie Kim, Andrew G Franks
Anetoderma is a rare benign elastolytic disorder that is characterized by focal loss of elastin fibers on histopathology and is often recalcitrant to treatment. We present a case of a patient with a 20-year history of pruritic and painful hyperpigmented atrophic papules clustered on the neck, axillae, inframammary folds, and right medial thigh. Although the histopathologyof her axillary lesions was consistent with anetoderma, her clinical presentation is unusual given the extent of involvement, reported pain and pruritus, and sharp demarcation of the distribution...
December 15, 2017: Dermatology Online Journal
https://www.readbyqxmd.com/read/29447657/generalized-hyperhidrosis-secondary-to-presumed-eccrine-gland-dysfunction-with-possible-apocrine-metaplasia
#8
Kumar Sukhdeo, Jenna Beasley, Alisa Femia, Randie Kim
We present a 57 year-old man presented with generalized hyperhidrosis and widespread, smooth, flesh colored papules on the torso and extremities.Histological examination from multiple biopsies demonstrated morphologic alteration of the eccrine glands with an apocrine phenotype, suggesting eitherapocrine metaplasia or the presence of "apoeccrine glands." The morphologic similarities between eccrine, apocrine, and apoeccrine as they relate to ourpatient's histologic findings are discussed. We consider secondary causes of generalized hyperhidrosis, which may also play a role in this patient's presentation...
December 15, 2017: Dermatology Online Journal
https://www.readbyqxmd.com/read/29447654/papular-mucinosis-or-localized-lichen-myxedematosis-lm-discrete-papular-type
#9
Mitalee P Christman, Kumar Sukhdeo, Randie H Kim, Shane Meehan, Evan Rieder, Kristen Lo Sicco, Andrew Franks
Lichen myxedematosus is condition characterized by localized areas of dermal deposition of mucin, presenting with firm papules localized to few areas of the body. The condition needs to be excluded from scleromyxedema, which, in addition to the firm papular eruption, has areas of induration and is usually associated with a monoclonal gammopathyand systemic symptoms. We present a 62-year-old woman with a several-year history of asymptomatic, firm papules over the face and arms with no evidence of thyroid disease or a monoclonal gammopathy,which is consistent with a diagnosis of localized lichen myxedematosus, the discrete papular variant...
December 15, 2017: Dermatology Online Journal
https://www.readbyqxmd.com/read/29447646/lichen-amyloidosis-of-the-scalp-and-forehead
#10
Yesul Kim, Michael D Ioffreda, Catherine G Chung
Lichen amyloidosis is a subtype of primary localized cutaneous amyloidosis (PLCA), which presents as discrete, firm, closely-set 1-3mm, dome-shapedbrown papules commonly involving the anterior aspect of shins and extensor surfaces of forearms. We present a case of an otherwise healthy man in his 30s with solitary facial involvement of lichen amyloidosis, which is very uncommon.
November 15, 2017: Dermatology Online Journal
https://www.readbyqxmd.com/read/29445576/solitary-orange-papule-on-the-back-of-a-middle-aged-man
#11
Shamir Geller, Melissa Pulitzer, Patricia L Myskowski
No abstract text is available yet for this article.
January 2018: Dermatology Practical & Conceptual
https://www.readbyqxmd.com/read/29445574/linear-verrucous-hemangioma-a-rare-case-and-dermoscopic-clues-to-diagnosis
#12
Aditi Dhanta, Payal Chauhan, Dilip Meena, Neirita Hazarika
Verrucous hemangioma (VH) is a rare, congenital and localized vascular malformation, which usually presents as warty, bluish, vascular papules, plaques, or nodules, mainly on the lower extremities. Linear presentation of the disease is rare. A deep biopsy is necessary to confirm the clinical diagnosis by histopathological examination, with dermoscopy acting as a useful tool for evaluating the precise vascular structure. Here, we report on a 13-year-old female child with linear VH presenting over her foot since infancy and dermoscopic findings of VH along with the clinical-pathologic features...
January 2018: Dermatology Practical & Conceptual
https://www.readbyqxmd.com/read/29445568/satisfactory-treatment-of-a-large-connective-tissue-nevus-with-intralesional-steroid-injection
#13
Nasrin Saki, Azadeh Dorostkar, Alireza Heiran, Fatemeh Sari Aslani
Collagenoma is a type of connective tissue nevi, a rare hamartomatous malformation characterized by the predominant proliferation of normal collagen fibers and normal, decreased, or increased elastic fibers. Collagenomas present as multiple or solitary, hereditary or sporadic, asymptomatic, skin-colored papules, nodules, and plaques with variable sizes, and are usually located on the trunk, arm, and back. Here, we report on a 14-year-old boy who presented with an isolated giant collagenoma of the frontal area that dramatically responded to intralesional triamcinolone acetonide...
January 2018: Dermatology Practical & Conceptual
https://www.readbyqxmd.com/read/29445567/an-unusual-lesion-on-the-nose-microvenular-hemangioma
#14
A Tulin Mansur, Gulsen Tukenmez Demirci, Eltaf A Ozbal Koc, Semsi Yildiz
Microvenular hemangioma (MVH) is an acquired, benign type of hemangioma that usually manifests itself as a solitary, slowly growing, red to violaceous, asymptomatic papule, plaque or nodule. It is typically located on the trunk or extremities of young adults. It can be difficult to differentiate MVH from other types of hemangioma and Kaposi sarcoma. Herein we report a case of MVH unusual for its location, age of onset, and morphologic features. A 62-year-old man complained of an asymptomatic, bluish-red discoloration on the tip of his nose that had been present for two years...
January 2018: Dermatology Practical & Conceptual
https://www.readbyqxmd.com/read/29444363/if-it-s-red-and-scaly-look-for-fungus-remember-cutaneous-protothecosis
#15
Ze-Hu Liu
A 34-year-old woman presented with a 5-year old history of unilateral facial erythematous plaque and scattered papules. The lesions continue to spread slowly. She complains mild pruritus. No medical history including diabetes or immunosuppression were recorded. Physical examination showed large area of well-demarcated erythematous plaque on the right cheek(Fig.A) with infiltrating pinpointed-flesh papules at the margin with less scales(Fig.B). This article is protected by copyright. All rights reserved.
February 14, 2018: Journal of the European Academy of Dermatology and Venereology: JEADV
https://www.readbyqxmd.com/read/29443700/new-onset-blue-black-papules-in-an-older-woman-question
#16
Nupur Patel, Colton B Nielson, Prasanna Sinkre, Kiran Motaparthi
No abstract text is available yet for this article.
February 6, 2018: American Journal of Dermatopathology
https://www.readbyqxmd.com/read/29443698/white-yellow-papules-on-the-neck-of-a-young-woman-challenge
#17
Kiran Motaparthi, Lori Ramirez, Brian J Hall
No abstract text is available yet for this article.
February 6, 2018: American Journal of Dermatopathology
https://www.readbyqxmd.com/read/29443697/t-lymphoblastic-leukemia-lymphoma-with-annular-skin-rash-and-epidermotropism
#18
Parisa Mansoori, Arash Taheri, Stacey S OʼNeill, Omar P Sangueza
Leukemia cutis is uncommon in patients with acute lymphoblastic leukemia. It typically presents with dermal papules or subcutaneous nodules, with no epidermal or upper papillary dermal involvement on histopathology. We present an unusual clinical presentation of leukemia cutis, with annular plaques and epidermotropism.
February 7, 2018: American Journal of Dermatopathology
https://www.readbyqxmd.com/read/29441410/-hyperkeratotic-papules-with-a%C3%A2-reticular-pattern-on-the-d%C3%A3-collet%C3%A3
#19
J K Winkler, C Fink, A Enk, F Toberer
No abstract text is available yet for this article.
February 13, 2018: Der Hautarzt; Zeitschrift Für Dermatologie, Venerologie, und Verwandte Gebiete
https://www.readbyqxmd.com/read/29441299/livedo-racemosa-reticulated-ulcerations-panniculitis-and-violaceous-plaques-in-a-46-year-old-woman
#20
Alfredo Agulló, Brian Hinds, Mónica Larrea, Ignacio Yanguas
Clinically amyopathic dermatomyositis (CADM) is a subset of dermatomyositis (DM) that has conventional cutaneous manifestations of DM, but paradoxically, little or no muscle involvement. In 2005, a novel antibody was described in association with CADM - anti-melanoma differentiation-associated gene 5 (anti-MDA5). Patients with this serologic marker have a characteristic mucocutaneous phenotype consisting of skin ulceration among other signs. We describe the case of a 46-year-old woman with CADM, elevated anti-MDA5 autoantibodies, and unusual clinical features (livedo racemosa, florid acral edema) among the classical phenotype of MDA5 DM (arthralgias, ulcerations, panniculitis) and classical DM lesions (Gottron papules, heliotrope rash)...
January 2018: Indian Dermatology Online Journal
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