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Full Text Journal Articles about
Eosinophilic Granuloma Histiocytosis X

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Pulmonary Langerhans Cell Histiocytosis Associated with Bronchogenic Carcinoma.

Muhammad F Khaliq, Muhammad M Noorani, Syed Maaz Tariq, Ashish Koirala, Hesham Mohamed,

Pulmonary Langerhans cell histiocytosis (PLCH, pulmonary eosinophilic granuloma) is a rare disease of clonal dendritic cells that primarily affects adults who smoke cigarettes. PLCH association with other malignancies is rarely reported. Herein, an unusual case of PLCH is presented with synchronous lung adenocarcinoma. A 76-year-old woman and chronic smoker was ... Read more >>

Cureus (Cureus)
[2020, 12(1):e6634]

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Suggested Case of Langerhans Cell Histiocytosis in a Cretaceous dinosaur.

Bruce M Rothschild, Darren Tanke, Frank Rühli, Ariel Pokhojaev, Hila May,

Susceptibility to diseases is common to humans and dinosaurs. Since much of the biological history of every living creature is shaped by its diseases, recognizing them in fossilized bone can furnish us with important information on dinosaurs' physiology and anatomy, as well as on their daily activities and surrounding environment. ... Read more >>

Sci Rep (Scientific reports)
[2020, 10(1):2203]

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MR imaging features of orbital Langerhans cell Histiocytosis.

Chunnan Wu, Kuncheng Li, Yan Hei, Pengyu Lan, Xuetao Mu,

BACKGROUND:To investigate the magnetic resonance imaging (MRI) features of orbital Langerhans cell histiocytosis (LCH) to improve diagnostic accuracy. METHODS:We retrospectively reviewed clinical manifestations and MRI findings of 23 patients with histopathology-confirmed LCH of the orbit. The findings were evaluated for the following: (a) symptoms, (b) disease duration, (c) location, (d) ... Read more >>

BMC Ophthalmol (BMC ophthalmology)
[2019, 19(1):263]

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Multifocal osteolytic lesions of jaw as a road map to diagnosis of brown tumor of hyperparathyroidism: A rare case report with review of literature.

Suchitra Gosavi, Harpreet Kaur, Pramod Gandhi,

Brown tumor is unifocal or multifocal bone disease which represents terminal stage of hyperparathyroidism (HPT)-dependent bone pathology. It is recognized as a component of metabolic bone disease called osteitis fibrosa cystica generalisata or Von Recklinghausen disease of bone. HPT was first described by Von Recklinghausen in 1891. Brown tumor diagnosis ... Read more >>

J Oral Maxillofac Pathol (Journal of oral and maxillofacial pathology : JOMFP)
[2020, 24(Suppl 1):S59-S66]

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Outcome of Surgery as Sole Treatment of Eosinophilic Granuloma of Jaws.

Saeed Nezafati, Javad Yazdani, Shahriar Shahi, Mahsa Mehryari, Emran Hajmohammadi,

Langerhans cell histiocytosis (LCH) is characterized by the congregation of proliferating langerhans cells (LC). Langerhans cells are a part of dendritic cell system of primary immune response that is responsible for presenting antigen to lymphocytes. Being a rare disease, the total incidence of LCH is reported to be 1 in ... Read more >>

J Dent (Shiraz) (Journal of dentistry (Shiraz, Iran))
[2019, 20(3):210-214]

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Imaging of skull vault tumors in adults.

Albert Pons Escoda, Pablo Naval Baudin, Paloma Mora, Mònica Cos, Javier Hernandez Gañan, José A Narváez, Carles Aguilera, Carles Majós,

The skull vault, formed by the flat bones of the skull, has a limited spectrum of disease that lies between the fields of neuro- and musculoskeletal radiology. Its unique abnormalities, as well as other ubiquitous ones, present particular features in this location. Moreover, some benign entities in this region may ... Read more >>

Insights Imaging (Insights into imaging)
[2020, 11(1):23]

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Diagnosis and treatment of Langerhans Cell Histiocytosis with bone lesion in pediatric patient: A case report.

Achmad Fauzi Kamal, Andi Praja Wira Yudha Luthfi,

Background:Langerhans cell histiocytosis (LCH) is a rare group of disorders without a well understood etiology. Known formerly as histiocytosis X, the disease has a wide spectrum of clinical presentations, including eosinophilic granuloma (solitary bone lesion), diabetes insipidus, and exophthalmos. Many of these patients initially present to orthopaedic surgeons, and misdiagnosis ... Read more >>

Ann Med Surg (Lond) (Annals of medicine and surgery (2012))
[2019, 45:102-109]

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Clinical analysis of Kimura's disease in 24 cases from China.

Guoliang Zhang, Xumao Li, Guangbin Sun, Yitan Cao, Nan Gao, Weidong Qi,

BACKGROUND:We reviewed details of Chinese Kimura's disease (KD) cases. A full clinical analysis was subsequently performed to improve the accuracy of clinical diagnosis and treatment of KD. METHODS:A total of 24 patients with pathologically confirmed KD treated between March 2008 and March 2018 were reviewed retrospectively for clinical and histopathological ... Read more >>

BMC Surg (BMC surgery)
[2020, 20(1):1]

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Langerhans cell histiocytosis of the hip in children.

Zied Jlalia, Dhia Kaffel,

Pan Afr Med J (The Pan African medical journal)
[2019, 33:230]

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Cytological Diagnosis of Rosai-Dorfman Disease: A Study of Twelve Cases with Emphasis on Diagnostic Challenges.

Rallapalli Rajyalakshmi, Mohammad Akhtar, Yarlagadda Swathi, Ranjani Chakravarthi, Jeeru Bhaskara Reddy, Maddirala Beulah Priscilla,

Context:Rosai-Dorfman disease, also known as Sinus histiocytosis with massive lymphadenopathy, is a benign proliferative disorder of histiocytes. It typically affects lymph nodes; however, extranodal disease is being increasingly reported. The latter entity poses exceptional diagnostic challenge clinico-radiologically by forming mass lesions. Fine needle aspiration cytology (FNAC) is the investigation of ... Read more >>

J Cytol (Journal of cytology)
[2020, 37(1):46-52]

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A case of multisystem Langerhans cell histiocytosis presenting as central diabetes insipidus.

P Daniel Nicholas, Ian Garrahy,

Langerhans cell histiocytosis (LCH) is a rare malignancy most commonly characterized by histiocytic infiltration of bone. LCH lesions in the skull place the adjacent central nervous system (CNS) at risk for involvement, which can manifest as central diabetes insipidus (CDI) when there is infiltration of the hypothalamic-pituitary axis. We present ... Read more >>

J Community Hosp Intern Med Perspect (Journal of community hospital internal medicine perspectives)
[2019, 9(6):515-517]

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Cervical Dystonia Mimics: A Case Series and Review of the Literature.

Srinivas Raju, Amogh Ravi, L K Prashanth,

Background:Cervical dystonia is mostly idiopathic in nature. However, a small subset of cases are mimics, leading to diagnostic pitfalls. There is paucity of literature on pseudodystonias affecting the cervical region. Method:We performed a retrospective review of patients attending a movement disorders clinic over a period of 7 years (2012-2018). Among ... Read more >>

Tremor Other Hyperkinet Mov (N Y) (Tremor and other hyperkinetic movements (New York, N.Y.))
[2019, 9:]

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A Newborn Female with a Diffuse Rash.

Zachary E Holcomb, Sherry H Yu, Tyler D Menge, Rosalynn M Nazarian, Chad J Jessup,

Langerhans cell histiocytosis is a rare and clinically heterogeneous group of dendritic histiocytic disorders with typical onset in the neonatal period or infancy, although it can present at any age. Histiocytes accumulate in one or more organs, leading to a variable clinical presentation of disease. We report a case of ... Read more >>

Dermatopathology (Basel) (Dermatopathology (Basel, Switzerland))
[2019, 6(3):189-194]

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Congenital self-healing langerhans cell histiocytosis: clinical and pathological characteristics.

Yu Pan, Xianfeng Zeng, Juan Ge, Xiaoyan Liu, Ying Chen, Donghua Zhou,

INTRODUCTION:Congenital Self-Healing Langerhans Cell Histiocytosis (CSHLCH) is rare, characterized by cutaneous lesions at birth or in the neonatal period, and absence of systemic lesions. MATERIALS AND METHODS:Skin biopsy was performed and the histologic examination of the skin section, routinely stained with hematoxylin-eosin. Paraffin sections were stained by immunohistochemical study which ... Read more >>

Int J Clin Exp Pathol (International journal of clinical and experimental pathology)
[2019, 12(6):2275-2278]

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Langerhans cell histiocytosis of the mandible: two case reports and literature review.

Dae-Seok Hwang, Jun Sang Lee, Uk-Kyu Kim, Hae Ryoun Park, Mi Heon Ryu, Ji Hye Lee, Yun-Hoa Jung, Gyoo Cheon Kim,

Langerhans cell histiocytosis (LCH) is a rare disorder characterized by the proliferation of dendritic cells resulting in local or systemic symptoms. The clinical symptoms of patients with Langerhans cell histiocytosis depend on the site and the degree of involvement. This article describes two case histories of unifocal bony Langerhans cell ... Read more >>

J Korean Assoc Oral Maxillofac Surg (Journal of the Korean Association of Oral and Maxillofacial Surgeons)
[2019, 45(3):167-172]

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Camurati-Engelmann Disease with Good Treatment Response to Losartan.

Mansoor Cherumkuzhiyil Abdulla,

Camurati-Engelmann disease (CED) or progressive diaphyseal dysplasia is a rare autosomal dominant inherited condition which belongs to the group of craniotubular hyperostosis. A 24-year-old man presented with insidious onset, progressive pain over both legs, and forearms for 3 years. He was born as the second child of a nonconsanguineous union ... Read more >>

Indian J Nucl Med (Indian journal of nuclear medicine : IJNM : the official journal of the Society of Nuclear Medicine, India)
[2019, 34(3):223-225]

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Langerhans cell histiocytosis: An enigmatic disease.

Anubha Jain, Sushil Kumar, Priyanka Aggarwal, Mohan Kumar, Vineeta Gupta,

Background:Langerhans cell histiocytosis (LCH) is a poorly understood disease with heterogeneous clinical presentation ranging from unifocal bony involvement to disseminated disease with life-threatening complications. Materials and Methods:The clinical profile, laboratory findings, treatment, and long-term outcome were retrieved from maintained medical records from January 2006 to January 2016 and were retrospectively ... Read more >>

South Asian J Cancer (South Asian journal of cancer)
[2019, 8(3):183-185]

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Langerhans cell histiocytosis of the jaw, a mimicker of osteomyelitis on CT and MR images: A retrospective analysis.

Jo-Eun Kim, Won-Jin Yi, Min-Suk Heo, Sam-Sun Lee, Soon-Chul Choi, Kyung-Hoe Huh,

Differential diagnosis of Langerhans Cell Histiocytosis (LCH) in the jaw is essential for early treatment including systemic therapy. Records of 17 patients (6 men and 11 women; mean age, 14 years) with histologically confirmed LCH were reviewed. All the lesions occurred in the mandible. Most of the cases (n=12) were ... Read more >>

Medicine (Baltimore) (Medicine)
[2019, 98(27):e16331]

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Langerhans cell histiocytosis presenting as eosinophilic granuloma of the bilateral forearms in an 8-year-old girl: a case report.

Salahoudine Idrissa, Hind Cherrabi, Boubacar Efared, Kassim Sidibé, Karima Attaraf, Lamiae Chater, Abderahmane Afifi,

BACKGROUND:Langerhans cell histiocytosis previously known as histiocytosis X is a rare disease of children and young adults with a very broad clinical spectrum. In children, its annual incidence is estimated between 0.2-0.5 per 100,000. CASE REPRESENTATION:An 8-year-old Moroccan girl with no known personal or family history presented to our institution ... Read more >>

J Med Case Rep (Journal of medical case reports)
[2019, 13(1):67]

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Recurrent pneumothorax, skin lesions and frequent urination.

Kunal Deokar, Ram Niwas, Nishant Chauhan, Naveen Dutt, Priyank Jain, Shahir Asfahan, Rajani Kumawat,

The causes of cystic lung diseases are varied. Proper evaluation is required for appropriate management. http://bit.ly/37J7dvE. ... Read more >>

Breathe (Sheff) (Breathe (Sheffield, England))
[2020, 16(1):190318]

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Retinal vasculitis with Chronic Recurrent Multifocal Osteomyelitis: a case report and review of the literature.

Victoria K Shanmugam, Marc Phillpotts, Timothy Brady, Monica Dalal, Shawn Haji-Momenian, Esma Akin, Kavita Nataranjan, Sean McNish, Donald S Karcher,

Background:Concurrent presentation of retinal vasculitis with mixed sclerotic and lytic bone lesions is rare. Case presentation:We present the case of a 37-year old woman with a several year history of episodic sternoclavicular pain who presented for rheumatologic evaluation due to a recent diagnosis of retinal vasculitis. We review the differential ... Read more >>

BMC Rheumatol (BMC rheumatology)
[2019, 3:29]

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Incidence and radiological pattern of eosinophilic granuloma: a retrospective study in a Chinese tertiary hospital.

Sha-Sha Zhao, Lin-Feng Yan, Xiu-Long Feng, Pang Du, Bao-Ying Chen, Wen-Ting Dong, Yi Gao, Jie-Bing He, Guang-Bin Cui, Wen Wang,

BACKGROUND:The incidence and radiological patterns of eosinophilic granuloma (EG) in China is not clear. We described the incidence, presentation, and imaging characteristics of Chinese EG patients in a tertiary hospital. METHODS:A retrospective chart review was performed from January 2004 to October 2017 at a single tertiary general hospital. Seventy-six patients ... Read more >>

J Orthop Surg Res (Journal of orthopaedic surgery and research)
[2019, 14(1):123]

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A Rare Case Report on Xanthogranulomatous Osteomyelitis of Hip Mimicking Tuberculosis and Review of Literature.

Subodh Pathak, Rakesh Gautam, Prince Pc, Priyank Bagtharia, Aryan Sharma,

Xanthogranulomatous osteomyelitis (XO) is a rare chronic inflammatory process characterized by the presence of a large number of lipid-containing macrophages with lymphocytes and plasma cells. We present a case of XO of the hip in a 50-year-old woman with pain in the left hip for 28 months. The patient had ... Read more >>

Cureus (Cureus)
[2019, 11(10):e5921]

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Characteristic Reconstitution of the Spinal Langerhans Cell Histiocytosis in Young Children.

Naoyuki Nakamura, Yutaka Inaba, Yoichi Aota, Jiro Machida, Tomoyuki Saito,

BACKGROUND:Pediatric Langerhans cell histiocytosis (LCH) often results in vertebral compression fracture. However, few reports have reported vertebral remodeling during the course of LCH. We aimed to investigate the longitudinal reconstitution and transformation of the affected vertebrae and the adjacent structures in young children with spinal LCH. METHODS:We recruited 13 patients, ... Read more >>

J Pediatr Orthop (Journal of pediatric orthopedics)
[2019, 39(4):e308-e311]

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Pulmonary Langerhans cell histiocytosis in adults: A case report.

Feng-Feng Wang, Ya-Shuang Liu, Wei-Bo Zhu, Yan-Dong Liu, Yao Chen,

BACKGROUND:Langerhans cell histiocytosis (LCH) is a rare disease of unknown aetiology. While it may affect any organ of the body, few cases of solitary lung involvement are published in the literature. Here, we report a rare case of pulmonary LCH (PLCH) in an adult. CASE SUMMARY:A 52-year-old male presented to ... Read more >>

World J Clin Cases (World journal of clinical cases)
[2019, 7(14):1892-1898]

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