Results 41 to 50 of about 8,935 (206)
LANGERHANS CELLS HISTIOCYTOSIS IN ONE FAMILY [PDF]
Acta Medica Iranica, 2004 Histiocytosis of Langerhans cells (class 1 histiocytosis) consists of a range of clinical manifestations, including bone eosinophilic granuloma, Hand-Schüller-Christian syndrome, and Letterer-Siwe disease. These syndromes represent a spectrum of severity
Sh. Ansari +1 more
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Adult Langerhans cell histiocytosis with pulmonary and colorectoanal involvement: a case report
Journal of Medical Case Reports, 2017 Background Langerhans cell histiocytosis is a rare systemic disease characterized by the abnormal overproduction of histiocytes that tend to infiltrate single or multiple organ systems leading to significant tissue damage. It mainly affects – by order of
Mohamad Jihad Mansour +4 more
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Clinical Case Reports, Volume 14, Issue 1, January 2026.ABSTRACT Ruptured hydatid cyst should be considered when encountering spontaneous pneumothorax and pneumomediastinum, especially in young patients in regions with high prevalence of hydatid cyst. Awareness of atypical signs ensures instant diagnosis, guiding appropriate surgical and medical treatment to prevent serious complications.
Farzaneh Akbari +5 more
wiley +1 more source
Clinical experience in an infant with Langerhans cell histiocytosis
Universidad Médica Pinareña, 2021 Introduction: Langerhans cell histiocytosis (LCH) or Histiocytosis X is a benign proliferative disease affecting dendritic cells. It presents a wide clinical spectrum, from isolated eosinophilic bone granuloma to multisystem involvement with multiple ...
Yamilka Pita Barrios +2 more
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Histiocytosis X: Langerhans’ Cell Histiocytosis
Hematology/Oncology Clinics of North America, 1987 Histiocytosis X is a complex and poorly understood entity. Nevertheless, it would appear as if certain themes are found recurrently throughout the literature dealing with this disease and a review of them serves as a useful summary. 1. Problems with Nomenclature.
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Orthopaedic Surgery, Volume 18, Issue 1, Page 53-65, January 2026.Robot‐assisted surgery facilitates precise path planning and osteotomy plane identification. With the combination of an orthopedic robot and intraoperative ultrasound or the da Vinci robot, it can enhance the precision and safety of bone tumor surgery. Furthermore, it can be integrated with patient‐specific cutting guides to minimize surgical duration.
Hanxiao Yin +9 more
wiley +1 more source
Tissue‐Resident Myeloid and Histiocytic Cells in Health and Disease: Novel Emerging Concepts
American Journal of Hematology, Volume 100, Issue 12, Page 2305-2319, December 2025.ABSTRACT Although all myeloid cells are considered to derive from hematopoietic stem cells, the cells in each myeloid lineage are heterogeneous populations, and their distribution and functions vary, depending on underlying physiologic and pathologic processes, age, sex, and genetic and epigenetic signatures.
Peter Valent +27 more
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Diagnostic problems and surgical treatment of histiocytosis X [PDF]
Medicinski Glasnik, 2007 A 16-year-old boy, with swelling and pain in the left submandibular region was treated at the Clinic for Maxillofacial Surgery. The x-ray examination showed destructive bone lesion of the mandibulae left side and oval lesions on the left hand bone and ...
Alkhalil M, A. Redžić, A. Smajilagić
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Secondary aneurysmal bone cyst in Langerhans cell histiocytosis: Case report, literature review
European Journal of Radiology Open, 2019 Langerhans cell histiocytosis (LCH) is a rare disease of the myeloid precursor cells, it predominantly occurs in the skull and long bones as unifocal bone lesions. Aneurysmal bone cysts (ABC) are benign, expansive and lytic bone. Reports of secondary ABC
P. Lomoro +6 more
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Extensive reactive cutaneous histiocytic infiltrate resembling non-Langerhans cell histiocytosis as the presenting sign of underlying vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic syndrome [PDF]
, 2023 Cynthia X. Wang +3 more
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