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Artykuły w czasopismach na temat „Cake – Juvenile literature”

Autor: Grafiati

Data publikacji: 27 lipca 2024

Data aktualizacji: 31 lipca 2025

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1

Dourado, Isadora. "Centro de Atendimento Juvenil Especializado (CAJE) e adolescentes em conflito com a lei no Distrito Federal: uma revisão de literatura." Revista do CEAM 8 (March 31, 2023): 118–28. https://doi.org/10.5281/zenodo.7787333.

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[Português] O objetivo deste trabalho foi revisar a literatura acadêmica existente sobre o Centro de Atendimento Juvenil Especializado (CAJE), local de aplicação de medidas de restrição de liberdade aos jovens e às jovens em conflito com a lei no Distrito Federal entre 1973 e 2014. A pergunta de pesquisa foi como a literatura descreve e analisa as funções das políticas públicas na adolescência. A revisão da literatura foi organizada segundo categorias analíticas para o material empírico analis

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2

Liu, Xin, Jingxi Wang, Yanglu Liu, et al. "High Intensity Focused Ultrasound Ablation for Juvenile Cystic Adenomyosis: Two Case Reports and Literature Review." Diagnostics 13, no. 9 (2023): 1608. http://dx.doi.org/10.3390/diagnostics13091608.

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Cystic adenomyosis is a rare type of uterine adenomyosis, mainly seen in young women, which is often characterized by severe dysmenorrhea. The quality of life and reproductive function of young women could be affected by misdiagnosis and delayed treatment. At present, there are no universal guidelines and consensus. We report two cases of patients with cystic adenomyosis in juveniles treated with high-intensity focused ultrasound (HIFU) ablation. In the first case, magnetic resonance imaging (MRI) indicated a cystic mass of 2.0 cm × 3.1 cm × 2.4 cm in the uterus. After she underwent HIFU treat

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3

Maalouf, Nadine Sophie, Akli Aouane, Patrick Hamel, Sara-Élizabeth Jean, Myrna Chababi-Atallah, and Carolina Lucena Fernandes. "Disseminated juvenile xanthogranulomas with ocular involvement: A case report and literature review." SAGE Open Medical Case Reports 10 (January 2022): 2050313X2211176. http://dx.doi.org/10.1177/2050313x221117693.

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Cutaneous juvenile xanthogranuloma is an uncommon disorder usually arising during infancy. Systemic involvement of juvenile xanthogranuloma remains rare, and there are no published guidelines to date on screening extracutaneous manifestations in these patients. Ocular involvement is the most common extracutaneous manifestation of juvenile xanthogranuloma. We present the case of an infant with disseminated juvenile xanthogranulomas and associated ocular involvement and present a review of literature, focusing on identifying risk factors for ocular and systemic involvement in disseminated cases.

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Vahabi-Amlashi, Sadegh, Masoumeh Hoseininezhad, and Zahra Tafazzoli. "Juvenile Xanthogranuloma: Case Report and Literature Review." International Medical Case Reports Journal Volume 13 (February 2020): 65–69. http://dx.doi.org/10.2147/imcrj.s240115.

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Wilbanks, William L. "Juvenile Killers: Case Examples and Academic Literature." Contemporary Psychology: A Journal of Reviews 36, no. 9 (1991): 748–49. http://dx.doi.org/10.1037/030131.

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Flor-de-Lima, Filipa, Mafalda Sampaio, Nahid Nahavandi, Susana Fernandes, and Miguel Leão. "Alsin Related Disorders: Literature Review and Case Study with Novel Mutations." Case Reports in Genetics 2014 (2014): 1–5. http://dx.doi.org/10.1155/2014/691515.

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Mutations in theALS2gene cause three distinct disorders: infantile ascending hereditary spastic paraplegia, juvenile primary lateral sclerosis, and autosomal recessive juvenile amyotrophic lateral sclerosis. We present a review of the literature and the case of a 16-year-old boy who is, to the best of our knowledge, the first Portuguese case with infantile ascending hereditary spastic paraplegia. Clinical investigations included sequencing analysis of the ALS2 gene, which revealed a heterozygous mutation in exon 5 (c.1425_1428del p.G477Afs*19) and a heterozygous and previously unreported varia

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7

Eleftheriades, Anna, Ermioni Tsarna, Konstantina Toutoudaki, et al. "Giant Juvenile Fibroadenoma: Case Report and Review of the Literature." Journal of Clinical Medicine 12, no. 5 (2023): 1855. http://dx.doi.org/10.3390/jcm12051855.

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Fibroadenomas are common benign breast tumors. Fibroadenomas that exceed 5 cm in diameter, weigh more than 500 g, or replace more than four-fifths of the breast are characterized as giant. A fibroadenoma diagnosed in patients during childhood or adolescence is characterized as juvenile. An extensive PubMed search of the literature in English up until August 2022 was performed. In addition, a rare case of a gigantic fibroadenoma in an 11-year-old premenarchal girl who was referred to our adolescent gynecology center is presented here. Eighty-seven cases of giant juvenile fibroadenomas have been

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8

Baisya, Ritasman, Phani Kumar Devarasetti, Ramakrishna Narayanan, and Liza Rajasekhar. "Posterior reversible encephalopathy syndrome in juvenile lupus- a case series and literature review." Lupus 31, no. 5 (2022): 606–12. http://dx.doi.org/10.1177/09612033221088207.

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Introduction: PRES, as a complication of juvenile lupus, is rarely reported in the literature. In this study, six juvenile lupus patients admitted with diagnosis of PRES were assessed on the basis of clinical characteristics, imaging findings, disease activity status, treatment response and prognosis. Methodology: Six juvenile (≤ 16 years) lupus patients with a diagnosis of PRES were included. Demographic, clinical, and laboratory features and outcomes of all six patients were noted. Literature review was performed on PubMed search forum. Search terms in English included Juvenile SLE, Lupus an

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9

Vuzitas, Alexis, and Claudiu Manea. "Juvenile nasopharyngeal angiofibroma – literature review and case series." Romanian Journal of Rhinology 8, no. 29 (2018): 17–24. http://dx.doi.org/10.2478/rjr-2018-0002.

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Abstract Juvenile nasopharyngeal angiofibroma is a rare benign tumour of vascular origin found in adolescent males, originating around the sphenopalatine foramen. Although the exact pathogenesis of the tumour is not yet known, natural history and growth patterns can be predicted. JNA progressively involves the nasopharynx, nasal cavity, paranasal sinuses, pterygopalatine fossa, infratemporal fossa and, in severe cases, an orbital or intracranial extension can be seen. Early diagnosis based on clinical examination and imaging is mandatory to ensure the best resectability of the tumour, as small

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10

Ziaee, Vahid, Mohammad Hassan Moradinejad, and Reyhaneh Bayat. "RHUPUS Syndrome in Children: A Case Series and Literature Review." Case Reports in Rheumatology 2013 (2013): 1–4. http://dx.doi.org/10.1155/2013/819629.

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Objective. Overlap of juvenile idiopathic arthritis (JIA) and juvenile systemic lupus erythematosus (JSLE) is a rare clinical condition in children. This condition has been described as RHUPUS syndrome. Prevalence of this syndrome and 3 cases are reported in this paper.Cases Presentation. During 10 years, 3 patients with SLE had chronic arthritis before or after diagnosis of SLE. Prevalence of this disorder in JSLE was 2.5%. Two patients were females and one of them was a male. According to our review, mean delay between chronic joint involvement and JSLE diagnosis was 50.1 months. In our case

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11

Sheth, Sharvin K., Amit C. Jhala, and Jay V. Shah. "Hirayama Disease: A Rare Case Report and Literature Review." Back Bone Journal 3, no. 2 (2022): 109–12. http://dx.doi.org/10.13107/bbj.2022.v03i02.048.

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Hirayama disease is a rare neurological condition and is characterized by a sporadic juvenile muscular atrophy of distal upper extremity in young males. The disease is more prevalent in Japan and other Asian countries, though a few cases have been reported in Western countries as well. It manifests as a self-limiting, gradually progressive atrophic weakness of forearm and hand. The anterior displacement of posterior dura during neck flexion leading to cervical cord atrophy has been hypothesized. We discuss a case of a 21-year-old male patient with progressive distal upper extremity weakness, d

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12

Muhammad, Juliawati, Yusnita Yusof, Imran Ahmad, Chen Hui Kew, Pei Yeing Teoh, and Nabilah Huda Hamzah. "Juvenile xanthogranuloma: A case report and literature review." Electronic Journal of General Medicine 19, no. 4 (2022): em380. http://dx.doi.org/10.29333/ejgm/12029.

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13

Lad, S., J. Seely, M. Elmaadawi, et al. "Juvenile Papillomatosis: A Case Report and Literature Review." Clinical Breast Cancer 14, no. 5 (2014): e103-e105. http://dx.doi.org/10.1016/j.clbc.2014.03.003.

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14

Ghanam, Ayad, Manal Azizi, Hind Zahiri, Aziza El Ouali, Abdeladim Babakhouya, and Maria Rkain. "Juvenile Xanthogranuloma: A Case Report with Literature Review." Open Journal of Pediatrics 14, no. 03 (2024): 531–35. http://dx.doi.org/10.4236/ojped.2024.143051.

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15

Le Donne, Mélanie, Océane Abattu, Claire Pernier, Emeline Durieux, and Anne-Gaëlle Bodard. "Impacted canine and ossifying fibroma: case report and literature review." Journal of Oral Medicine and Oral Surgery 25, no. 4 (2019): 37. http://dx.doi.org/10.1051/mbcb/2019018.

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Introduction: An impacted tooth is a permanent tooth that has a completely developed root but which has failed to erupt. Many etiologies can lead to impaction, including a mechanical obstacle, such as benign tumor. Observation: An 11-year-old girl was referred for the avulsion of the left mandibular permanent canine, which was impacted. A radiolucent lesion with ground glass opacity was found on the eruption pathway of the tooth. Anterior radiographs showed the lesion that seemed to be the cause of the impacted canine. Anatomopathological examination revealed the lesion to be a juvenile trabec

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16

Al Hammadi, Anwar, and Miriam Hakim. "Pachydermodactyly: Case Report and Review of the Literature." Journal of Cutaneous Medicine and Surgery 11, no. 5 (2007): 185–87. http://dx.doi.org/10.2310/7750.2007.00024.

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Background: Pachydermodactyly is a benign form of digital fibromatosis usually presenting in male adolescent patients as asymptomatic nodules on the lateral aspects of the proximal interphalangeal joints of the fingers. It is commonly misdiagnosed as a juvenile rheumatologic condition. Objective and Conclusion: Recognition of the features of this disease will assist dermatologists and rheumatologists in making the diagnosis of this rare condition.

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17

Cypel, Tatiana Karine Simon, and Ronald Melvin Zuker. "Juvenile Xanthogranuloma: Case Report and Review of the Literature." Canadian Journal of Plastic Surgery 16, no. 3 (2008): 175–77. http://dx.doi.org/10.1177/229255030801600309.

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Huang, Y. ‐W, and T. ‐F Tsai. "Juvenile‐onset pustular psoriasis: case series and literature review." British Journal of Dermatology 182, no. 3 (2019): 816–17. http://dx.doi.org/10.1111/bjd.18473.

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19

Damasceno, Evilane Costa Cesário, and Mayara Carvalho de Lima. "TRANSMISSÃO GERACIONAL FAMILIAR DA VIOLÊNCIA SEXUAL INFANTO-JUVENIL: UM OLHAR DA GESTALT-TERAPIA." Revista Fenexis: Estudos Fenomenológicos Existenciais 1, no. 1 (2023): 1–19. https://doi.org/10.29327/2485992.1.1-1.

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O presente estudo teve como objetivo compreender as possíveis repercussões da transmissão geracional intrafamiliar na reprodução da violência sexual infanto-juvenil. Para isso, foi utilizado como método a pesquisa de abordagem qualitativa e exploratória, visando explorar os materiais que se encontram no meio científico através da pesquisa bibliográfica. Foi adotada a revisão integrativa como recurso metodológico, utilizando-se de fontes bibliográficas como publicações em periódicos, a partir das bases de dados Google Scholar, Scielo, CAFe e Scribd. Com base na literatura encontrada, foi organi

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20

Velletrani, Gianluca, Beatrice Francavilla, and Valentina Rosati. "Adult onset Xanthogranuloma presenting as a solitary laryngeal localization: case report and review of literature." Archive of Clinical Cases 9, no. 4 (2022): 145–49. http://dx.doi.org/10.22551/2022.37.0904.10221.

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Juvenile Xanthogranuloma (XG) is a rare disorder that belongs to the heterogeneous group of histiocytic neoplasms, characterized by a clonal expansion of non-Langerhans cell histiocytes that share a dermal macrophage phenotype. Although the head and neck region is the most common reported site of involvement by the Juvenile Xanthogranuloma family, laryngeal localization is extremely rare. We report a unique case of Adult Onset Xanthogranuloma with subglottic localization, presenting as a solitary laryngeal mass without other systemic or cutaneous lesions. A review of the previously described c

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21

John Esteban Verdugo Parra, Kevin Fabricio Orellana Barros, Hugo Xavier Guamán Roldan, and Janneth Alexandra Villavicencio Benavides. "Juvenile nasopharyngeal angiofibroma: A clinical case report and a literature review." World Journal of Advanced Research and Reviews 22, no. 3 (2024): 1693–700. http://dx.doi.org/10.30574/wjarr.2024.22.3.1835.

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Juvenile nasopharyngeal angiofibroma (JNA) is a benign tumor with locally aggressive behavior, given the significant epistaxis it causes, frequent complications, and therapeutic complexity presented by this condition, diagnosis and treatment should be thorough; it occurs exclusively in adolescent males and accounts for 0.5%-0.05% of all head and neck tumors. This case corresponds to an 18-year-old patient with progressive respiratory difficulty over 2 years, nasal obstruction, and epistaxis. Clinical and imaging studies revealed a diagnosis of JNA at stage IIb according to Radkowski's classifi

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22

John, Esteban Verdugo Parra, Fabricio Orellana Barros Kevin, Xavier Guamán Roldan Hugo, and Alexandra Villavicencio Benavides Janneth. "Juvenile nasopharyngeal angiofibroma: A clinical case report and a literature review." World Journal of Advanced Research and Reviews 22, no. 3 (2024): 1693–700. https://doi.org/10.5281/zenodo.14760318.

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Juvenile nasopharyngeal angiofibroma (JNA) is a benign tumor with locally aggressive behavior, given the significant epistaxis it causes, frequent complications, and therapeutic complexity presented by this condition, diagnosis and treatment should be thorough; it occurs exclusively in adolescent males and accounts for 0.5%-0.05% of all head and neck tumors. This case corresponds to an 18-year-old patient with progressive respiratory difficulty over 2 years, nasal obstruction, and epistaxis. Clinical and imaging studies revealed a diagnosis of JNA at stage IIb according to Radkowski's classifi

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23

Güneş, Yasin Celal, Pelin Seher Öztekin, Tülin Değirmenci, et al. "Juvenile papillomatosis: A case report." Turkish Journal of Surgery 40, no. 2 (2024): 178–82. http://dx.doi.org/10.47717/turkjsurg.2022.4745.

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Juvenile papillomatosis (JP) is a very rare benign proliferative breast disease, especially in young women under 30 years of age. Its etiology is not clear yet. Although some patients have breast cancer in their family history, up to 10% breast cancer can develop in the follow-up of JP patients. In this pathology, which is diagnosed with biopsy, history, clinical and radiological findings help in diagnosis. In this case report, a 37-year-old patient diagnosed with JP will be discussed in the light of the literature.

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Nikumbh, D. B., S. R. Desai, P. S. Madan, N. J. Patil, and J. V. Wader. "Bilateral Giant Juvenile Fibroadenomas of Breasts:A Case Report." Pathology Research International 2011 (May 30, 2011): 1–4. http://dx.doi.org/10.4061/2011/482046.

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Juvenile fibroadenoma constitutes only 4% of the total fibroadenomas. The incidence of giant juvenile fibroadenomas is found to be only 0.5% of all the fibroadenomas. Bilateral giant juvenile fibroadenomas are extremely rare, and only four cases have been reported in the literature. To the best of our knowledge, we are presenting the fifth case of bilateral giant juvenile fibroadenomas in a 12-year-old prepubertal girl. The diagnosis was made on fine-needle aspiration cytology which was confirmed on histopathology. In this paper, we present this rare case to illustrate the diagnosis and manage

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25

Nair, Preeti, Anil Kumar, Karthik Hegde, and Shiba Neelakantan. "Psammomatoid Juvenile Ossifying Fibroma: A Case Report with Literature Review." Journal of Indian Academy of Oral Medicine and Radiology 22 (September 15, 2010): S53—S57. http://dx.doi.org/10.5005/jp-journals-10011-1071.

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Rao, Raghavendra, KanagalaChowdary Neethu, C. Balachandran, and Sathish Pai. "Juvenile IgA pemphigus: A case report and review of literature." Indian Journal of Dermatology, Venereology, and Leprology 82, no. 4 (2016): 439. http://dx.doi.org/10.4103/0378-6323.181467.

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Takami, Akiyoshi, Yasuaki Tatsumi, Katsuhisa Sakai, et al. "Juvenile Hemochromatosis: A Case Report and Review of the Literature." Pharmaceuticals 13, no. 8 (2020): 195. http://dx.doi.org/10.3390/ph13080195.

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Juvenile hemochromatosis (JH), type 2A hemochromatosis, is a rare autosomal recessive disorder of systemic iron overload due to homozygous mutations of HJV (HFE2), which encodes hemojuvelin, an essential regulator of the hepcidin expression, causing liver fibrosis, diabetes, and heart failure before 30 years of age, often with fatal outcomes. We report two Japanese sisters of 37 and 52 years of age, with JH, who showed the same homozygous HJV I281T mutation and hepcidin deficiency and who both responded well to phlebotomy on an outpatient basis. When all reported cases of JH with homozygous HJ

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Bharani, AnjaliT, Mohini Harshey, Randhir Khurana, and Swati Raipurkar. "A rare case of juvenile dermatomyositis and review of literature." Indian Journal of Paediatric Dermatology 18, no. 2 (2017): 107. http://dx.doi.org/10.4103/2319-7250.202994.

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Gadient, Paul, Jeffrey Bolton, and Vinay Puri. "Juvenile Myasthenia Gravis: Three Case Reports and a Literature Review." Journal of Child Neurology 24, no. 5 (2009): 584–90. http://dx.doi.org/10.1177/0883073808325651.

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Raj, Divya, and R. Rathy. "Juvenile Xanthogranuloma: A Case Report and Review of the Literature." International journal of odontostomatology 12, no. 3 (2018): 327–31. http://dx.doi.org/10.4067/s0718-381x2018000300327.

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Shimoyama, Tetsuo, Norio Horie, and Fumio Ide. "Juvenile xanthogranuloma of the lip: Case report and literature review." Journal of Oral and Maxillofacial Surgery 58, no. 6 (2000): 677–79. http://dx.doi.org/10.1016/s0278-2391(00)90167-8.

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Rogers, Nicole E., Patricia K. Farris, and Alun R. Wang. "Juvenile Chondrodermatitis Nodularis Helicis: A Case Report and Literature Review." Pediatric Dermatology 20, no. 6 (2003): 488–90. http://dx.doi.org/10.1111/j.1525-1470.2003.20606.x.

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Oza, Vikash S., Thomas Stringer, Caren Campbell, et al. "Congenital-type juvenile xanthogranuloma: A case series and literature review." Pediatric Dermatology 35, no. 5 (2018): 582–87. http://dx.doi.org/10.1111/pde.13544.

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Pradhan, Sushmita. "Case Reports on Juvenile Xanthogranuloma and Brief Review of Literature." Science Journal of Clinical Medicine 6, no. 5 (2017): 82. http://dx.doi.org/10.11648/j.sjcm.20170605.14.

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Singh, Suman, Neelam, and Rashmi K Raina. "Role of fine needle aspiration cytology in the diagnosis of juvenile xanthogranuloma in adult: Case report and review of the literature." IP Archives of Cytology and Histopathology Research 6, no. 2 (2021): 128–31. http://dx.doi.org/10.18231/j.achr.2021.031.

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Juvenile xanthogranuloma(JXG) is an uncommon benign histiocytic cutaneous lesion which is seen primarily in first two decades of life. There is not much literature available on its cytology. We present a case of solitary juvenile xanthogranuloma in a 43 years old female located above left nasal ala which was diagnosed on Fine needle aspiration cytology and subsequently confirmed on histology. Characteristic cytological features favored a diagnosis of juvenile xanthogranuloma.

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Venkatesh, Kusuma, Karishma Pillarisetty, and Sreedhara Murthy B. N. "Juvenile polyposis syndrome with extraintestinal anomalies: report of a rare case with review of literature." International Journal of Research in Medical Sciences 5, no. 2 (2017): 720. http://dx.doi.org/10.18203/2320-6012.ijrms20170183.

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Juvenile polyposis coli is a rare condition in children with neoplastic potential having an incidence of about 1 in 1,00,000 population. A minority of such patients have extraintestinal abnormalities like cardiac and pulmonary arteriovenous malformations. Juvenile polyposis is a disorder of hamartomatous polyposis syndrome having a malignant potential. The progression of hamartomatous polyp to carcinoma is still elucidated when compared to the understanding of transformation of an adenomatous polyp into a carcinoma via a gatekeeper defect. Here is the report of a rare case of Juvenile polyposi

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Khmelevska, N. "Reintegration of minors in juvenile justice." Analytical and Comparative Jurisprudence, no. 4 (September 14, 2023): 430–34. http://dx.doi.org/10.24144/2788-6018.2023.04.69.

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The article analyzes the concept of reintegration of minors in juvenile justice. Punitive approach is not effective in working with minors. It is important to understand that the quality of the criminal process in which minors find themselves depends on their future and whether they will commit criminal offenses in the future. It is also necessary to remember that minor victims and witnesses also need reintegration, but different from minor offenders. It is indicated that different terminology is used in the literature to denote the process of reintegration, namely «resocialization», «reintegr

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38

Nagata, Masumi, Keisuke Jimbo, Nobuyasu Arai, et al. "An Isolated Intestinal Juvenile Polyp Diagnosed by Abdominal Ultrasonography and Resected by Double-Balloon Endoscopy: A Case Report and Literature Review." Diagnostics 13, no. 3 (2023): 494. http://dx.doi.org/10.3390/diagnostics13030494.

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Juvenile polyps, typically localized in the rectum and sigmoid colon, are a common cause of pediatric bloody stool. An isolated small intestinal juvenile polyp is uncommon and generally difficult to diagnose. The first case of an isolated juvenile polyp diagnosed by abdominal ultrasonography before acute abdomen had developed and resected by double-balloon endoscopy is presented along with a review of previous reports including this case. A two-year-old Japanese boy was referred to our institute for further evaluation of anemia persisting from one year of age. Laboratory findings showed mild i

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Bouchalova, Katerina, Hana Flögelova, Pavel Horak, et al. "Juvenile Primary Sjögren Syndrome in a 15-Year-Old Boy with Renal Involvement: A Case Report and Review of the Literature." Diagnostics 14, no. 3 (2024): 258. http://dx.doi.org/10.3390/diagnostics14030258.

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Juvenile primary Sjögren syndrome (pSS) with renal involvement is extremely rare, reported approximately in 50 children, predominantly girls. Here, we present the first reported case of a male child with juvenile pSS with ocular surface disease (previously keratoconjunctivitis sicca), submandibular salivary gland involvement, and tubulointerstitial nephritis. First, two symptoms were clinically apparent at presentation. We illustrate here that kidney involvement in pSS should be actively looked for, as juvenile pSS may be associated with asymptomatic renal involvement. Immunophenotyping of per

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40

Mears, Daniel P. "Evaluation Issues Confronting Juvenile Justice Sentencing Reforms: A Case Study of Texas." Crime & Delinquency 44, no. 3 (1998): 443–63. http://dx.doi.org/10.1177/0011128798044003007.

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Many states currently are implementing “get tough” sentencing reforms in juvenile justice. Surprisingly, however, little attention has been given to evaluation issues identified by the adult justice sentencing literature as critical to assessments of efficacy. Analysis of one recent juvenile justice sentencing reform in Texas—determinate sentencing—provides an opportunity to highlight such issues and to demonstrate their relevance to assessment of other states' juvenile justice sentencing reforms. This article identifies the failure to attend adequately to design, implementation, use, and asse

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Kundu, Narayan Chandra, Moushumi Sen, KM Nazmul Islam Joy, and Feroj Ahmed Quraish. "Juvenile Myasthenia Gravis: A Case Report and Review of Literatures." Bangladesh Journal of Neuroscience 29, no. 1 (2013): 64–69. http://dx.doi.org/10.3329/bjn.v29i1.56173.

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Juvenile myasthenia gravis (JMG) is a rare autoimmune disorder of childhood. Pediatric presentation of MG is more common in Oriental than in Caucasian populations. JMG need to be differentiated from congenital myasthenia gravis which do not have haan autoimmune basis. An 11 years old girl presented with drooping of eye lids which was more marked at the later part of day and was gradually progressive . She had complained of double vision. She had no family history of myasthenia gravis. Ice pack test, repetitive nerve stimulation test, and anti acetylcholine receptor antibody test support the di

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Orgeron, Rhett. "Complications of refractory juvenile dermatomyositis: a case report and literature review." MOJ Clinical & Medical Case Reports 11, no. 1 (2021): 8–12. http://dx.doi.org/10.15406/mojcr.2021.11.00371.

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We present a 29-year-old male with a history of treatment resistant juvenile dermatomyositis (JDM). The patient was admitted for complaints of nausea, diarrhea and abdominal pain and was subsequently found to have intestinal perforation on imaging. The patient had also exhibited classic dermatologic findings alongside rare dermato-pathological manifestations of JDM on examination; likely consequences of his underlying disease process. This case serves to present these rare findings and analyze the similarities of JDM and adult dermatomyositis (DM). In addition, overall diagnosis and treatment

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Skarda, J., V. Ticha, M. Tichy, M. Perelman, and J. Kopolovic. "Pulmonary Manifestations of Juvenile Laryngotracheal Papillomatosis: Case Report and Literature Review." Open Pathology Journal 3, no. 1 (2009): 131–33. http://dx.doi.org/10.2174/1874375700903010131.

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Ndhlovu, Elijah, Hui Deng, Jun Dai, Xiyuan Dong, Lili Liu, and Biao Chen. "Juvenile granulosa cell tumor in pregnancy: case series and literature review." Archives of Gynecology and Obstetrics 305, no. 5 (2021): 1299–310. http://dx.doi.org/10.1007/s00404-021-06283-5.

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Muzaffer, Mohammed. "Juvenile Systemic Lupus Erythematosus and Glioblastoma:A Case Report and Literature Review." مجلة جامعة الملك عبدالعزيز-العلوم الطبية 20, no. 3 (2013): 111–18. http://dx.doi.org/10.4197/med.20-3.10.

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Deblaere, Lieselot, Wouter Froyman, Thierry Van den Bosch, et al. "Juvenile cystic adenomyosis: A case report and review of the literature." Australasian Journal of Ultrasound in Medicine 22, no. 4 (2019): 295–300. http://dx.doi.org/10.1002/ajum.12171.

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Richards, Masters, Cassandra Albertin, Anne-Marie Priebe, and Rachel Miller. "Refractory Juvenile Catamenial Pneumothorax: A Case Report and Brief Literature Review." Journal of Pediatric and Adolescent Gynecology 29, no. 2 (2016): 187. http://dx.doi.org/10.1016/j.jpag.2016.01.069.

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Ladha, Malika A., and Richard M. Haber. "Giant Juvenile Xanthogranuloma: Case Report, Literature Review, and Algorithm for Classification." Journal of Cutaneous Medicine and Surgery 22, no. 5 (2018): 488–94. http://dx.doi.org/10.1177/1203475418777734.

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Juvenile xanthogranuloma (JXG) is a member of the non-Langerhans cell group of proliferative disorders of mononuclear phagocytes. JXG is a benign tumour of histiocytic cells. Classic JXG is divided into 2 main clinical subtypes: dome-shaped papules (<0.5 cm) and single/multiple nodules (<2.0 cm). A rare variant is referred to as giant; this term encompasses JXG lesions larger than 2.0 cm. In this article, we report a case of a congenital cutaneous giant JXG. In addition, we reviewed and analyzed all cases (n = 51) of giant JXG reported in the English literature. We propose an algorithm f

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Imerci, Ahmet, Umut Canbek, Sema Haghari, Levent Sürer, and Muge Kocak. "Idiopathic juvenile osteoporosis: A case report and review of the literature." International Journal of Surgery Case Reports 9 (2015): 127–29. http://dx.doi.org/10.1016/j.ijscr.2015.02.043.

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Thomas, Jean E., Meena Moossavi, Darius R. Mehregan, Wendy L. McFalda, and Michael J. Mahon. "Juvenile hyaline fibromatosis: a case report and review of the literature." International Journal of Dermatology 43, no. 11 (2004): 785–89. http://dx.doi.org/10.1111/j.1365-4632.2004.02239.x.

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