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合計: 33 |
|
| PMID (PMCID) | ||
|---|---|---|
|
29243280 |
MALE | Adult |
| Mixed histiocytosis: A case report and published work review. | ||
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Li Z, Li Y, Liu W, Li J, Wang L. J Dermatol. 2018;45(4):491-495. |
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| Mixed histiocytosis, the concomitant occurrence of Langerhans cell histiocytosis and non-Langerhans cell histiocytosis in a single patient, is exceptional. | ||
|
30094268 (6080074) |
OTHER | |
| Simultaneous Bilateral Spontaneous Pneumothorax in an Adult Patient With Pulmonary Langerhans Cell Histiocytosis: A Case Report. | ||
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Karamouzos V, Prokakis C, Kosmopoulou F, Karanikolas E, Kalogeropoulou C, Aretha D, Panagiotopoulos N, Koletsis E, Velissaris D. J Investig Med High Impact Case Rep. 2018;6:2324709618792945. |
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| A review of pulmonary Langerhans cell histiocytosis and treatment options in cases of pneumothorax due to lung histiocytosis is also presented in this report. | ||
|
28977321 (5417814) |
FEMALE | Infant |
| LATE-ONSET SELF-HEALING LANGERHANS CELL HISTIOCYTOSIS: REPORT OF A VERY RARE ENTITY. | ||
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Afsar FS, Ergin M, Ozek G, Vergin C, Karakuzu A, Seremet S. Rev Paul Pediatr. 2017;35(1):115-119. |
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| Self-healing Langerhans cell histiocytosis, which is characterized by clonal proliferation of Langerhans cells and presents with cutaneous lesions, is a rare self-limited variant of histiocytosis and can only be diagnosed retrospectively, after the patient remains free from systemic involvement for several years. | ||
|
28547972 |
MALE | Young Adult |
| Puzzle histiocytosis (solitary mononuclear xanthogranuloma with LCH component). A case report. | ||
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Woszczyna-Mleczko K, Kowalik A, Harazin-Lechowska A, Bobkiewicz P, Marszalek A, Rys J. Pol J Pathol. 2016;67(4):415-420. |
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| The puzzle histiocytosis composed of juvenile xanthogranuloma and Langerhans cell histiocytosis was diagnosed. | ||
|
26588339 (4894786) |
FEMALE | Middle Aged |
| Combined Cutaneous Rosai-Dorfman Disease and Localized Cutaneous Langerhans Cell Histiocytosis Within a Single Subcutaneous Nodule. | ||
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Litzner BR, Subtil A, Vidal CI. Am J Dermatopathol. 2015;37(12):936-9. |
||
| Langerhans cell histiocytosis (LCH) is a clonal histiocytosis with a wide spectrum of presentations ranging from isolated skin or bone disease to multisystem involvement. | ||
|
25434508 |
MIXED_SAMPLE | Adult |
| Endocrine changes in histiocytosis of the hypothalamic-pituitary axis. | ||
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Toro Galvan S, Planas Vilaseca A, Michalopoulou Alevras T, Torres Diaz A, Suarez Balaguer J, Villabona Artero C. Endocrinol Nutr. 2015;62(2):72-9. |
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| Histiocytosis is characterized by proliferation of cells from the mononuclear phagocyte system, and may be divided into Langerhans cell histiocytosis (LCH) and non-Langerhans cell histiocytosis (including Erdheim-Chester disease [ECD]). | ||
|
23996873 |
OTHER | |
| A case of isolated cutaneous Rosai-Dorfman-Syndrome. | ||
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Rizwan MM, Chhabra G, Mishra A, Kapadia S, Rai R, Gill H. Gulf J Oncolog. 2013;1(14):87-9. |
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| RDD has been described as a dynamic entity in the spectrum of histiocytosis with non-Langerhans cell histiocytosis at one end and Langerhans cell histiocytosis at the other. | ||
|
22565457 |
MALE | Infant, Newborn |
| Congenital self-healing histiocytosis presenting as blueberry muffin baby: a case report and literature review. | ||
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Popadic S, Brasanac D, Arsov B, Nikolic M. Indian J Dermatol Venereol Leprol. 2012;78(3):407. |
||
| Congenital self-healing Langerhans cell histiocytosis (CSHLCH), also called as Hashimoto-Pritzker disease, is a rare, benign variant of histiocytosis. | ||
|
18094573 |
MIXED_SAMPLE | Child |
| [Bone marrow fibrin-ring granuloma: review of 24 cases]. | ||
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Chung HJ, Chi HS, Cho YU, Jang S, Park CJ. Korean J Lab Med. 2007;27(3):182-7. |
||
| EBV-associated group comprised chronic active EBV infection, EBV-associated hemophagocytic histiocytosis, acute EBV infection, EBV-associated lymphoproliferative disease, and Langerhans' cell histiocytosis. | ||
|
16243135 |
FEMALE | Infant |
| Solitary cutaneous dendritic cell tumor in a child: role of dendritic cell markers for the diagnosis of skin Langerhans cell histiocytosis. | ||
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Weiss T, Weber L, Scharffetter-Kochanek K, Weiss JM. J Am Acad Dermatol. 2005;53(5):838-44. |
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| CSHRH is a spontaneously regressing, benign form of Langerhans cell histiocytosis (LCH) and was thought to be a histiocytosis consisting of precursor Langerhans cells. | ||
|
16786802 |
MIXED_SAMPLE | |
| [Endocrinology complications of Langerhans cell histiocytosis]. | ||
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Kaminska H, Korpal-Szczyrska M, Polczynska K, Dorant B, Birkholz D. Przegl Lek. 2005;62(12):1577-9. |
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| Fine needle aspiration cytology of the focus localized in the left lobe of thyroid gland and nearest enlarged lymph nodes revealed diffuse infiltrate by the large histiocytosis confirming Langerhans cell histiocytosis like in the skin histological specimen biopsy. | ||
|
11142791 |
FEMALE | Adult |
| [Unifocal eosinophilic granuloma of the temporal bone (Langerhans cell histiocytosis]. | ||
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Cajade Frias JM, Cajade Bao D, Lozano Ramirez A, Castro Vilas C, Vaamonde Lago P, Labella Caballero T. Acta Otorrinolaringol Esp. 2000;51(6):525-9. |
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| Eosinophilic granuloma is one of the diseases of unknown etiology traditionally known as histiocytosis X and now called histiocytosis of the Langerhans cells since it has been found to originate by proliferation of this cell line. | ||
|
9185228 |
FEMALE | |
| Deep juvenile xanthogranuloma: an unusual presentation. | ||
|
Neveling U, Kahn LB, Valderrama E, Poustchi-Amin M, Uckan D, Shende A. Pediatr Pathol Lab Med. 1997;17(3):503-11. |
||
| Differentiation of JXG from other childhood histiocytosis syndromes, especially Langerhans' cell histiocytosis (LCH), is important. | ||
|
9251959 |
FEMALE | Adult |
| Langerhans cell histiocytosis of vulva and cervix in a 19-year-old woman. | ||
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Stentella P, Cipriano L, Covello R, Faticanti Scucchi L, Frega A. Gynecol Obstet Invest. 1997;44(1):67-9. |
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| We present a case of a 19-year-old woman with Langerhans cell histiocytosis of mandible and maxilla with subsequent cervical and vulvar histiocytosis. | ||
|
9740830 |
FEMALE | Infant |
| [Acquired regressive cutaneous non-Langerhans-cell histiocytosis in an infant]. | ||
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Campourcy M, Moreau-Cabarrot A, Gorguet B, Samalens G, Daste B, Eclache F, Bazex J. Ann Dermatol Venereol. 1997;124(2):167-70. |
||
| Four diagnosis were possible in our case: histiocytosis X, self-healing congenital histiocytosis, benign cephalic histiocytosis, juvenile xanthogranuloma. | ||
|
8739984 |
MIXED_SAMPLE | Adult |
| Eosinophilic histiocytosis. Histopathology and immunohistochemistry. | ||
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Helton JL, Maize JC. Am J Dermatopathol. 1996;18(2):111-7. |
||
| In addition, eosinophilic histiocytosis lacks multinucleated histiocytes and the atypical histiocyte with a reniform nucleus, findings that are characteristic of histiocytosis X. | ||
|
8543320 |
MALE | Middle Aged |
| Erdheim-Chester disease: a case report with immunohistochemical and biochemical examination. | ||
|
Ono K, Oshiro M, Uemura K, Ota H, Matsushita Y, Ijima S, Iwase T, Uchida M, Katsuyama T. Hum Pathol. 1996;27(1):91-5. |
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| These results suggested that the disease was part of the spectrum of histiocytosis but was different from Langerhans cell histiocytosis. | ||
|
9033881 |
FEMALE | Middle Aged |
| [Imaging of Erdheim-Chester disease]. | ||
|
Gomez C, Diard F, Chateil JF, Moinard M, Dousset V, Rivel J. J Radiol. 1996;77(12):1213-21. |
||
| Erdheim-Chester disease is a form of Histiocytosis which involves the adults and is distinct from Histiocytosis X. | ||
|
8561825 |
MALE | Adult |
| [Langerhans cell histiocytosis of the temporal bone]. | ||
|
Issing PR, Ernst A, Kempf HG, Buhr T, Lenarz T. Laryngorhinootologie. 1995;74(11):702-6. |
||
| The localized form of the Langerhans cell histiocytosis was referred to earlier as eosinophilic granuloma, which has the best prognosis of all histiocytosis syndromes concerning survival. | ||
|
1908575 |
MALE | Infant, Newborn |
| Congenital histiocytosis. A heterogeneous group of diseases, one presenting as so-called congenital self-healing histiocytosis. | ||
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Kodet R, Elleder M, De Wolf-Peeters C, Mottl H. Pathol Res Pract. 1991;187(4):458-66. |
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| A diffuse cellular positivity of alpha-mannosidase in juvenile xanthogranuloma and congenital self-healing histiocytosis differed from a typical perinuclear globular positivity of this enzyme in Langerhans cell histiocytosis. | ||