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Isolated hypothalamic-pituitary langerhans’ cell histiocytosis in female adult: A case report
RATIONALE: Langerhans cell histiocytosis (LCH) is characterized by clonal proliferation of immature dendritic cells, mainly affects children. LCH in adult sellar region is extremely rare. In literature, optimal treatments remain unclear and only a few cases of LCH were treated using surgery. Here, w...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6336579/ https://www.ncbi.nlm.nih.gov/pubmed/30633157 http://dx.doi.org/10.1097/MD.0000000000013853 |
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author | Tan, Huiwen Yu, Kai Yu, Yerong An, Zhengmei Li, Jianwei |
author_facet | Tan, Huiwen Yu, Kai Yu, Yerong An, Zhengmei Li, Jianwei |
author_sort | Tan, Huiwen |
collection | PubMed |
description | RATIONALE: Langerhans cell histiocytosis (LCH) is characterized by clonal proliferation of immature dendritic cells, mainly affects children. LCH in adult sellar region is extremely rare. In literature, optimal treatments remain unclear and only a few cases of LCH were treated using surgery. Here, we present a rare case of isolated hypothalamic-pituitary LHC in female adult. We focused on elucidating the clinical manifestations and immunohistochemical features of LCH, and exploring the proper treatment in adults. PATIENT CONCERNS: A 50-year-old woman was admitted to our hospital, presenting with polydipsia and polyuria for over 3 months. DIAGNOSES: Radiological studies revealed lesions (0.5 × 0.9 × 0.4 cm) on posterior pituitary and enlarged pituitary stalk, which was moderately enhanced on contrast magnetic resonance imaging (MRI) of sellar region. In biopsy, pathological examination of Langerhans cells were observed with positive S-100 protein and Ki-67 antigen markers, findings were sufficient to establish a diagnosis of central nervous system (CNS) LCH. INTERVENTIONS: The patient with LCH restricted in the sellar region received both surgery and chemotherapy. Gamma knife radiosurgery was performed after diagnosed as central diabetes insipidus (CDI) induced by pituitary lesion. And tumorectomy was performed 5 years later. However, in the latest MRI in 2017, the nodular shadow became larger (about 1.4 cm), chemotherapy and further systemic therapy were given. OUTCOMES: At 12-month follow-up, no local reoccurrence was noticed. LESSONS: For LCH, though difficult to be diagnosed and none defined standard therapeutic approach to adults, surgery should be considered if there are neurological symptoms or histological diagnosis. The present study showed that some manifestations can be meaningful when central nervous system (CNS) is involved. For complex diseases in the sellar region, multi-disciplinary team (MDT) model of diagnosis and treatment should be helpful for better clinical efficacy. |
format | Online Article Text |
id | pubmed-6336579 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-63365792019-01-24 Isolated hypothalamic-pituitary langerhans’ cell histiocytosis in female adult: A case report Tan, Huiwen Yu, Kai Yu, Yerong An, Zhengmei Li, Jianwei Medicine (Baltimore) Research Article RATIONALE: Langerhans cell histiocytosis (LCH) is characterized by clonal proliferation of immature dendritic cells, mainly affects children. LCH in adult sellar region is extremely rare. In literature, optimal treatments remain unclear and only a few cases of LCH were treated using surgery. Here, we present a rare case of isolated hypothalamic-pituitary LHC in female adult. We focused on elucidating the clinical manifestations and immunohistochemical features of LCH, and exploring the proper treatment in adults. PATIENT CONCERNS: A 50-year-old woman was admitted to our hospital, presenting with polydipsia and polyuria for over 3 months. DIAGNOSES: Radiological studies revealed lesions (0.5 × 0.9 × 0.4 cm) on posterior pituitary and enlarged pituitary stalk, which was moderately enhanced on contrast magnetic resonance imaging (MRI) of sellar region. In biopsy, pathological examination of Langerhans cells were observed with positive S-100 protein and Ki-67 antigen markers, findings were sufficient to establish a diagnosis of central nervous system (CNS) LCH. INTERVENTIONS: The patient with LCH restricted in the sellar region received both surgery and chemotherapy. Gamma knife radiosurgery was performed after diagnosed as central diabetes insipidus (CDI) induced by pituitary lesion. And tumorectomy was performed 5 years later. However, in the latest MRI in 2017, the nodular shadow became larger (about 1.4 cm), chemotherapy and further systemic therapy were given. OUTCOMES: At 12-month follow-up, no local reoccurrence was noticed. LESSONS: For LCH, though difficult to be diagnosed and none defined standard therapeutic approach to adults, surgery should be considered if there are neurological symptoms or histological diagnosis. The present study showed that some manifestations can be meaningful when central nervous system (CNS) is involved. For complex diseases in the sellar region, multi-disciplinary team (MDT) model of diagnosis and treatment should be helpful for better clinical efficacy. Wolters Kluwer Health 2019-01-11 /pmc/articles/PMC6336579/ /pubmed/30633157 http://dx.doi.org/10.1097/MD.0000000000013853 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | Research Article Tan, Huiwen Yu, Kai Yu, Yerong An, Zhengmei Li, Jianwei Isolated hypothalamic-pituitary langerhans’ cell histiocytosis in female adult: A case report |
title | Isolated hypothalamic-pituitary langerhans’ cell histiocytosis in female adult: A case report |
title_full | Isolated hypothalamic-pituitary langerhans’ cell histiocytosis in female adult: A case report |
title_fullStr | Isolated hypothalamic-pituitary langerhans’ cell histiocytosis in female adult: A case report |
title_full_unstemmed | Isolated hypothalamic-pituitary langerhans’ cell histiocytosis in female adult: A case report |
title_short | Isolated hypothalamic-pituitary langerhans’ cell histiocytosis in female adult: A case report |
title_sort | isolated hypothalamic-pituitary langerhans’ cell histiocytosis in female adult: a case report |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6336579/ https://www.ncbi.nlm.nih.gov/pubmed/30633157 http://dx.doi.org/10.1097/MD.0000000000013853 |
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