Langerhans cell histiocytosis associated with myelodysplastic syndrome in adults

2006 ◽  
Vol 33 (2) ◽  
pp. 171-174 ◽  
Author(s):  
Steven D. Billings ◽  
Christine P. Hans ◽  
Brian L. Schapiro ◽  
Robert W. Martin ◽  
David Fivenson ◽  
...  
Keyword(s):  
Myelodysplastic Syndrome ◽  
Langerhans Cell Histiocytosis ◽  
Langerhans Cell

Cladribine‐related myelodysplastic syndrome in Langerhans cell histiocytosis

2019 ◽  
Vol 61 (4) ◽  
pp. 419-421 ◽  
Author(s):  
Yukiko Oh ◽  
Tomomi Hayase ◽  
Takane Ito ◽  
Yuta Kawahara ◽  
Akira Morimoto
Keyword(s):  
Myelodysplastic Syndrome ◽  
Langerhans Cell Histiocytosis ◽  
Langerhans Cell

Association Between High-grade Myelodysplastic Syndrome and Cutaneous Langerhans Cell Histiocytosis Suggested by Next-Generation Sequencing

2020 ◽  
Vol 156 (7) ◽  
pp. 817 ◽  
Author(s):  
Sharad Khurana ◽  
Jason C. Sluzevich ◽  
Rong He ◽  
Danielle K. Reimer ◽  
Mohamed A. Kharfan-Dabaja ◽  
...  
Keyword(s):  
Next Generation Sequencing ◽  
Myelodysplastic Syndrome ◽  
Langerhans Cell Histiocytosis ◽  
Langerhans Cell ◽  
High Grade ◽  
Next Generation ◽  
Generation Sequencing

scholarly journals Case Report: Multisystem Langerhans Cell Histiocytosis (LCH) and Myelodysplastic Syndrome (MDS) in a 13-Month-Old Female

2021 ◽  
Vol 31 (3) ◽  
pp. 181
Author(s):  
Dian Sukma Hanggara ◽  
Desyi Desyi
Keyword(s):  
Myelodysplastic Syndrome ◽  
Langerhans Cell Histiocytosis ◽  
Cytokine Production ◽  
Bone Marrow Aspiration ◽  
Maculopapular Rash ◽  
Langerhans Cell ◽  
Patient Case ◽  
Skin Redness ◽  
Childhood Type ◽  
Positive Results

<p>Langerhans Cell Histiocytosis or LCH and Myelodysplastic syndrome or MDS in children are rare diseases. It is estimated to be 1 to 4 cases per 1 million population and less than 5% of hematologic cases. MDS in LCH can occur due to genetic predisposition, impaired cytokine production, or secondary to chemotherapy.  The article reported a patient case of a 13-month-old female who came to hospital with paleness since two weeks before admission. The patient also experienced skin redness, abdominal distention, and weight loss. From the physical examination, anemia, maculopapular rash, and hepatosplenomegaly were obtained. From the laboratory test, anemia of hypochromic anisopoikilocytosis, monocytosis, thrombocytopenia, and hypoalbuminemia were obtained. On examination of bone marrow aspiration, MDS with Refractory Cytopenia of Childhood type or RCC was obtained. Positive results confirmed the diagnosis of Langerhans Cell Histiocytosis on CD68 and S100 in histopathological examinations.</p>

Langerhans cell histiocytosis and thyroid carcinoma

1998 ◽  
Vol 138 (5) ◽  
pp. 909-910 ◽  
Author(s):  
Marzano ◽  
Gasparini ◽  
Grammatica ◽  
De Juli ◽  
Caputo
Keyword(s):  
Thyroid Carcinoma ◽  
Langerhans Cell Histiocytosis ◽  
Langerhans Cell

Cytogenetic abnormalities in PHA-stimulated lymphocytes from patients with Langerhans cell histiocytosis

2000 ◽  
Vol 111 (1) ◽  
pp. 258-262 ◽  
Author(s):  
Susi Scappaticci ◽  
Cesare Danesino ◽  
Elena Rossi ◽  
Catherine Klersy ◽  
Gian Mario Fiori ◽  
...  
Keyword(s):  
Langerhans Cell Histiocytosis ◽  
Langerhans Cell ◽  
Cytogenetic Abnormalities

Radiologic manifestation of pulmonary Langerhans' cell histiocytosis

1993 ◽  
Vol 29 (5) ◽  
pp. 973
Author(s):  
Jong Sung Kim ◽  
Duk Ja Bang ◽  
Hyun Chul Rhim ◽  
Seok Chol Jeon ◽  
Seung Ro Lee ◽  
...  
Keyword(s):  
Langerhans Cell Histiocytosis ◽  
Langerhans Cell ◽  
Pulmonary Langerhans Cell Histiocytosis
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