Indeterminate cell tumor (Histiocytosis)
Saudi Journal of Medicine and Medical Sciences, 2013 Indeterminate cell tumor (ICT; histiocytosis) is a rare disorder characterized by accumulation of histiocytes that do not fulfill the phenotypic criteria designated for Langerhans cells (LC).
Ayesha Ahmed +6 more
doaj +3 more sources
Indeterminate Cell Histiocytosis – Case Report and Review of Literature [PDF]
Serbian Journal of Dermatology and Venereology, 2018 Introduction. Indeterminate cell histiocytosis is a rare proliferative disorder of indeterminate dendritic cells, reported in only 50 case reports so far.
A. Vojvodić +2 more
semanticscholar +3 more sources
Indeterminate Cell Histiocytosis: Report of a Case
Acta Medica Iranica, 2014 Indeterminate cell histiocytosis is a very rare disorder of histiocytes proliferation. It has both Langerhans and non-Langerhans cell histiocytosis immunophenotypic features.
Alireza Ghanadan +8 more
doaj +2 more sources
A Case of Indeterminate Cell Histiocytosis
Nishi Nihon Hifuka, 2020 Seisho Sato +9 more
semanticscholar +3 more sources
Indeterminate Cell Histiocytosis in Children: A Case Report.
Actas Dermo-Sifiliográficas (English Edition), 2017 A. Sahuquillo-Torralba +3 more
semanticscholar +4 more sources
A case of indeterminate cell histiocytosis successfully treated with thalidomide [PDF]
Chinese Journal of Dermatologysemanticscholar +3 more sources
Post‐scabietic nodules: Mimicker of infantile indeterminate cell histiocytosis and potential diagnostic pitfall [PDF]
Journal of cutaneous pathology, 2020 Indeterminate cell histiocytosis (ICH) is an extremely rare disease and little is known about its etiology. Patients usually present with nodular, dermal proliferations of indeterminate cells, which characteristically resemble Langerhans cells but lack ...
Kristen N Ruby +3 more
semanticscholar +2 more sources
Indeterminate cell histiocytosis that presented clinically as benign cephalic histiocytosis [PDF]
Dermatology Online Journal, 2015 Indeterminate cell histiocytosis (ICH) is a rare, heterogeneous disorder that is characterized by immunophenotypic features of both Langerhans cell histiocytosis (LCH) and non-LCH. We describe a 12-month-old boy with a four-month history of asymptomatic, small, pink-tan papules on his face.
Haimovic, Adele +4 more
openaire +5 more sources
Orbital indeterminate cell histiocytosis
OrbitAn 8-year-old female presented to the oculoplastics clinic with 3 months of left upper eyelid fullness and edema. Examination showed a mass in the left anterior superior orbit with erythema. Imaging demonstrated a well-circumscribed superolateral orbital
Angela J. Oh +6 more
semanticscholar +3 more sources
Utilizing Computer-assisted Planning for Split Calvarial Bone Cranioplasty of an Infant With Occipital Langerhans Cell Histiocytosis [PDF]
Plastic and Reconstructive Surgery, Global OpenSummary:. Langerhans cell histiocytosis is frequently characterized by lytic calvarial lesions, periodically necessitating cranioplasty in infant patients.
Jordan R. Whittles, BS +5 more
doaj +2 more sources