Results 81 to 90 of about 31,396 (267)

Novel Histopathologic Features of Diffuse Blue‐Gray Hyperpigmentation Associated With Kratom Use: A Case Report and Literature Review

open access: yesJournal of Cutaneous Pathology, EarlyView.
ABSTRACT Background Drug‐induced hyperpigmentation accounts for 10%–20% of acquired pigmentary disorders and can be misdiagnosed for other causes such as melasma, post inflammatory changes, or heavy metal deposition. Kratom (Mitragyna speciosa), a Southeast Asian plant with an opioid‐like profile, has been increasingly used in the United States for ...
Rita Kamoua   +4 more
wiley   +1 more source

Lepra Bacilla in Foamy Histiocytes in Bone Marrow

open access: yes, 2002
lepra bacilla in foamy histiocytes in bone marrow ...
Lawrence, Christine
core  

Overall weighted sensitivity, specificity, positive likelihood ratios, negative likelihood ratios, diagnostic OR and AUC of caseation, confluent granulomas and ulcers lined by epithelioid histiocytes.

open access: yes, 2014
Overall weighted sensitivity, specificity, positive likelihood ratios, negative likelihood ratios, diagnostic OR and AUC of caseation, confluent granulomas and ulcers lined by epithelioid histiocytes.
You-Ming Li (5660824)   +3 more
core   +1 more source

A Recurrent Indurated Plaque on the Thigh

open access: yes
JEADV Clinical Practice, EarlyView.
Tram T. Tran   +3 more
wiley   +1 more source

A Rare Case of Cutaneous Crystal‐Storing Histiocytosis With Kappa Light Chain Restriction and Unusual BCL6 Expression

open access: yesJournal of Cutaneous Pathology, EarlyView.
ABSTRACT Crystal‐storing histiocytosis (CSH) is a rare histopathologic phenomenon characterized by the accumulation of crystalline material within histiocytes, most often associated with lymphoplasmacytic or plasma cell neoplasms. Cutaneous involvement is uncommon and may present diagnostic challenges.
Liangli Wang   +8 more
wiley   +1 more source

Primary intraosseous manifestation of Rosai-Dorfman disease: 2 cases and review of literature

open access: yesJournal of the Belgian Society of Radiology, 2014
Rosai-Dorman disease (RDD) is a rare disorder of proliferative histiocytes with an unknown etiology. It is also known as sinus histiocytosis with massive lymphadenopathy. Most patients present with painless cervical lymphadenopathy due to accumulation of
H M Duijsens   +4 more
doaj   +1 more source

Foamy Macrophages and Blue Histiocytes as Diagnostic Clues to Acid Sphingomyelinase Deficiency [PDF]

open access: yes
Acid sphingomyelinase deficiency; Bone marrow pathology; Blue histiocytesDeficiencia de esfingomielinasa ácida; Patología de la médula ósea; Histiocitos azulesDeficiència d'esfingomielinasa àcida; Patologia de la medul·la òssia; Histiòcits blausWe report
Ribell Bachs, Mònica   +5 more
core   +1 more source

A Growing Dark Mass in a Patient With a History of Trauma

open access: yes
JEADV Clinical Practice, EarlyView.
Takahiro Hase   +7 more
wiley   +1 more source

An Atypical Skin Presentation of Adult‐Onset Still's Disease With Histological Description: A Case Report

open access: yesJournal of Cutaneous Pathology, EarlyView.
ABSTRACT Adult‐onset Still's disease (AOSD) is an auto inflammatory disorder with a variable clinical presentation, and without a pathognomonic diagnostic test, characterized by high spiking fever, arthralgia/arthritis, a suggestive skin rash, elevated white blood cell count 10 G/L (> 80% neutrophils), elevated ferritin, with glycosylated ferritin < 20%
M. Nordmann   +7 more
wiley   +1 more source

Chronic Pruritic Papular Eruption in an Elderly Man

open access: yes
JEADV Clinical Practice, EarlyView.
Filipe Monteiro   +6 more
wiley   +1 more source

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