Results 11 to 20 of about 69,333 (214)

Systemic Mastocytosis

open access: yesThe American Journal of the Medical Sciences, 2011
Systemic mastocytosis (SM) is a clonal disorder of hematopoietic system characterized by abnormal growth and accumulation of mast cells in various tissues. Its clinical spectrum ranges from mild disease to an aggressive course with life-threatening conditions.
Didem, Ozdemir   +2 more
openaire   +3 more sources

Nodular mastocytosis: a case study

open access: yesVestnik Dermatologii i Venerologii, 2017
A case study of nodular mastocytosis is described. Tacrolimus was used to treat skin manifestations of mastocytosis.
E. V. Pavlova   +4 more
doaj   +2 more sources

Clinical features of mastocytosis at pediatric patients

open access: yesVestnik Dermatologii i Venerologii, 2017
Mastocytosis is relevant to heterogeneous disease group characterized with redundant accumulation and proliferation of mast cells in tissues. The skin form of mastocytosis is mainly occurs in children.
D. V. Proshutinskaya, O. S. Makoveckaya
doaj   +2 more sources

Melanoma and Mastocytosis

open access: yesOpen Access Macedonian Journal of Medical Sciences, 2019
There are numerous cases reports and studies confirming the enhanced incidence of melanoma among patients with mastocytosis, especially with systemic mastocytosis. These two diseases are arising from two different types of cells; melanoma arises from neural crest cells and mastocytosis from hematopoietic stem cells.
Vojvodic, Aleksandra   +13 more
openaire   +4 more sources

PEDIATRIC MASTOCYTOSIS

open access: yesHematology/Oncology Clinics of North America, 2000
Pediatric mastocytosis presents with heterogeneous cutaneous lesions and symptoms that are caused by increased numbers of tissue mast cells. In contrast with adult patients with mastocytosis, the course of pediatric patients is usually transient. Therefore, it has long been speculated that pediatric and adult mastocytosis may be based on different ...
Hartmann, Karin, Metcalfe, Dean D.
openaire   +4 more sources

Childhood Pseudoxanthomatousmastocytosis; Report of two cases

open access: yesIndian Journal of Dermatopathology and Diagnostic Dermatology, 2018
Cutaneous mastocytosis (CM) is a mast cell proliferative disorder that commonly affects pediatric population. It has various clinical forms such as urticaria pigmentosa, solitary mastocytoma, telangiectasia macularis eruptiva perstans, diffuse CM, and ...
Bhabani S. T. P. Singh   +3 more
doaj   +3 more sources

MASTOCYTOSIS [PDF]

open access: yesDermatologic Clinics, 2001
Mastocytosis represents a heterogeneous group of clinical disorders resulting from the infiltration of mast cells in the skin and other organs. Although mastocytosis was first described over 130 years ago, the pathophysiologic mechanisms responsible for this disease have been identified only recently.
M D, Tharp, B J, Longley
  +8 more sources

Bullous mastocytosis

open access: yesIndian Journal of Dermatology, 2007
Mastocytosis is a condition characterized by the disorderly infiltration of mast cells in several tissues and comprises many different clinical situations varying from indolent cutaneous forms to malignant and systemic conditions. Bullous mastocytosis is
Nayak Surajit   +3 more
doaj   +1 more source

Mastocytosis. General concepts, view on patient management, examples of clinical course of the disease

open access: yesZdorovʹe Rebenka, 2022
Background. Mastocytosis is a disease characterized by the presence of mast cells in various organs. The skin is affected most often. Almost every patient diagnosed with mastocytosis has skin lesions.
O.L. Statkevych, T.V. Sviatenko
doaj   +1 more source

Neuropsychiatric, cognitive and sexual impairment in mastocytosis patients

open access: yesOrphanet Journal of Rare Diseases, 2021
Background Mastocytosis is a rare disease characterised by the accumulation and/or proliferation of abnormal mast cells (MCs) in one or several organs. It may present with a number of different symptoms that involve various organ systems.
Fatma Jendoubi   +5 more
doaj   +1 more source

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