Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1967 1
1975 1
1979 1
1980 1
1981 1
1983 2
1984 1
1985 3
1987 1
1988 1
1989 3
1990 4
1991 1
1992 3
1993 1
1994 3
1995 5
1996 4
1997 5
1998 4
2000 1
2001 4
2002 3
2003 2
2004 4
2005 2
2006 3
2007 2
2008 3
2009 5
2010 4
2011 2
2012 6
2013 4
2014 2
2015 5
2017 6
2018 6
2019 6
2020 4
2021 5
2022 2
2023 3
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

119 results

Results by year

Filters applied: . Clear all
Page 1
Histiocytic disorders.
McClain KL, Bigenwald C, Collin M, Haroche J, Marsh RA, Merad M, Picarsic J, Ribeiro KB, Allen CE. McClain KL, et al. Nat Rev Dis Primers. 2021 Oct 7;7(1):73. doi: 10.1038/s41572-021-00307-9. Nat Rev Dis Primers. 2021. PMID: 34620874 Free PMC article. Review.
Prior classification schemes align disease designation with terminal phenotype: for example, Langerhans cell histiocytosis (LCH) shares CD207(+) antigen with physiological epidermal Langerhans cells. LCH, Erdheim-Chester disease (ECD), juvenile xanthogranuloma (JXG) and Ro …
Prior classification schemes align disease designation with terminal phenotype: for example, Langerhans cell histiocytosis (LCH) shares CD20 …
Cutaneous manifestations in neurofibromatosis type 1.
Miraglia E, Moliterni E, Iacovino C, Roberti V, Laghi A, Moramarco A, Giustini S. Miraglia E, et al. Clin Ter. 2020 Sep-Oct;171(5):e371-e377. doi: 10.7417/CT.2020.2242. Clin Ter. 2020. PMID: 32901776 Free article. Review.
Other skin manifestations included: lipoma (6.2%), nevus anemicus (3.9%), psoriasis (3.4%), spilus nevus (3.2%), juvenile xanthogranuloma (3.2%), vitiligo (2.3%), Becker's nevus (1.9%), melanoma (0.7%) and poliosis (0.5%). ...
Other skin manifestations included: lipoma (6.2%), nevus anemicus (3.9%), psoriasis (3.4%), spilus nevus (3.2%), juvenile xanthogranuloma …
Necrobiotic xanthogranuloma.
Mehregan DA, Winkelmann RK. Mehregan DA, et al. Arch Dermatol. 1992 Jan;128(1):94-100. Arch Dermatol. 1992. PMID: 1739294 Review.
We reviewed 32 cases of necrobiotic xanthogranuloma and 16 cases from the world literature. Necrobiotic xanthogranuloma is a destructive dermal and subcutaneous xanthogranuloma that most frequently involves the face (periorbital region) and trunk. ...
We reviewed 32 cases of necrobiotic xanthogranuloma and 16 cases from the world literature. Necrobiotic xanthogranuloma is a d …
Adult Xanthogranuloma, Reticulohistiocytosis, and Rosai-Dorfman Disease.
Chisolm SS, Schulman JM, Fox LP. Chisolm SS, et al. Dermatol Clin. 2015 Jul;33(3):465-72; discussion 473. doi: 10.1016/j.det.2015.03.011. Dermatol Clin. 2015. PMID: 26143426 Review.
Adult xanthogranuloma presents most commonly as an orange-tan firm solitary nodule with no systemic manifestations. Recently, some cases have been reported in conjunction with lymphoproliferative disorders. Adult reticulohistiocytosis classically presents as …
Adult xanthogranuloma presents most commonly as an orange-tan firm solitary nodule with no systemic manifestations. Recently, …
Primary histiocytic dermatoses.
Ringel E, Moschella S. Ringel E, et al. Arch Dermatol. 1985 Dec;121(12):1531-41. Arch Dermatol. 1985. PMID: 2998286 Review.
The malignant histiocytosis with erythrophagocytosis, the pseudomalignant histiocytic diseases (such as sinus histiocytosis with massive lymphadenopathy and regressing atypical histiocytosis), and the solitary lesions with histologic malignant and atypical storiform histiocytosis …
The malignant histiocytosis with erythrophagocytosis, the pseudomalignant histiocytic diseases (such as sinus histiocytosis with massive lym …
Adult Xanthogranulomatous Disease of the Orbit: Clinical Presentations, Evaluation, and Management.
Ortiz Salvador JM, Subiabre Ferrer D, Pérez Ferriols A. Ortiz Salvador JM, et al. Actas Dermosifiliogr. 2017 Jun;108(5):400-406. doi: 10.1016/j.ad.2016.12.005. Epub 2017 Mar 3. Actas Dermosifiliogr. 2017. PMID: 28262109 Free article. Review. English, Spanish.
Adult xanthogranulomatous disease of the orbit refers to a heterogeneous group of clinical syndromes with differing degrees of systemic involvement and distinct prognoses. ...There are 4 clinical forms of xanthogranulomatous disease of the orbit: adult xanthogranulo …
Adult xanthogranulomatous disease of the orbit refers to a heterogeneous group of clinical syndromes with differing degrees of system …
Cutaneous disseminated xanthogranuloma in an adult: case report and review of the literature.
Asarch A, Thiele JJ, Ashby-Richardson H, Norden PS. Asarch A, et al. Cutis. 2009 May;83(5):243-9. Cutis. 2009. PMID: 19537282 Review.
The condition is typified by the formation of reddish to yellow papules and nodules that are usually solitary. Xanthogranuloma rarely occurs in adults with immunohistochemical features similar to those seen in juvenile XG. Lesions in the adult form seen in ju …
The condition is typified by the formation of reddish to yellow papules and nodules that are usually solitary. Xanthogranuloma rarely …
The clinical spectrum of xanthomatous lesions of the eyelids.
Baykal C, Polat Ekinci A, Yazganoglu KD, Buyukbabani N. Baykal C, et al. Int J Dermatol. 2017 Oct;56(10):981-992. doi: 10.1111/ijd.13637. Epub 2017 May 13. Int J Dermatol. 2017. PMID: 28500693 Review.
Among these, Langerhans cell histiocytosis, diffuse normolipemic xanthoma, and non-Langerhans cell histiocytoses (papular xanthoma, juvenile xanthogranuloma, xanthoma disseminatum, adult-onset xanthogranuloma, adult-onset asthma and periocular xanth …
Among these, Langerhans cell histiocytosis, diffuse normolipemic xanthoma, and non-Langerhans cell histiocytoses (papular xanthoma, juvenile …
Cutaneous Hematolymphoid and Histiocytic Proliferations in Children.
Gru AA, Dehner LP. Gru AA, et al. Pediatr Dev Pathol. 2018 Mar-Apr;21(2):208-251. doi: 10.1177/1093526617750947. Pediatr Dev Pathol. 2018. PMID: 29607757 Review.
Although mycosis fungoides is the most frequent form of cutaneous lymphoma in adults, it is very rare in children. Because lymphoblastic leukemias and lymphomas are more frequent in the pediatric setting, cutaneous leukemic infiltrates are relatively common in this age-gro …
Although mycosis fungoides is the most frequent form of cutaneous lymphoma in adults, it is very rare in children. Because lymphoblas …
Juvenile xanthogranuloma.
Hernandez-Martin A, Baselga E, Drolet BA, Esterly NB. Hernandez-Martin A, et al. J Am Acad Dermatol. 1997 Mar;36(3 Pt 1):355-67; quiz 368-9. doi: 10.1016/s0190-9622(97)80207-1. J Am Acad Dermatol. 1997. PMID: 9091465 Review.
Juvenile xanthogranuloma (JXG) is a benign, self-healing disorder characterized by solitary or multiple yellow-red nodules on the skin and, occasionally, in other organs. It is predominantly a disease of infancy or early childhood, although adults may also be affect …
Juvenile xanthogranuloma (JXG) is a benign, self-healing disorder characterized by solitary or multiple yellow-red nodules on the ski …
119 results