Langerhans cell histiocytosis of the frontal bone with unexpected manifestations: Rare case report
Langerhans cell histiocytosis (LCH) is a disease caused by clonal expansion of myeloid precursors that differentiate into specialized dendritic cells. A 21-year-old female came to our hospital complaining of tachycardia, high temperature, and tumor formation in the frontal region with a fistula. The...
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description | Langerhans cell histiocytosis (LCH) is a disease caused by clonal expansion of myeloid precursors that differentiate into specialized dendritic cells.
A 21-year-old female came to our hospital complaining of tachycardia, high temperature, and tumor formation in the frontal region with a fistula. The examination of the thyroid gland and other systems was normal. The radiological investigations showed a severe lytic osseous lesion with aggressive destruction of the bone. The ultrasound imaging of the thyroid gland revealed that the thyroid was generally hypoechoic and heterogeneous because of many small hypoechoic focuses. In addition, the blood perfusion increased in the gland. The laboratory investigations were within normal expect C-reactive protein, free T4, and TSH. The surgery was indicated. The patient underwent an excision of the mass by a specialist in neurosurgery. The histopathological examination of the excised mass revealed LCH (eosinophilic granuloma). After 6 months, the patient underwent cranioplasty. The follow-up was uneventful for 3 months until the patient suffered from hyperthyroidism.
LCH can form in any part of the body, and cause many symptoms depending on its location. Even though hyperthyroidism is a rare and unexpected symptom of LCH.
LCH is a disease with broad-spectrum manifestations, so it should be a differential diagnosis in bone, thyroid, skin, and other organ lesions. In addition, thyroid ultrasonography and laboratory investigations are important methods to estimate thyroid functions and determine the clinical classification of the disease.
•LCH is a disease with broad-spectrum manifestations, so it should be a differential diagnosis in bone, thyroid, skin, and other organ lesions.•Thyroid ultrasonography and laboratory investigations are important methods to estimate thyroid functions and determine the clinical classification of the disease.•More studies are needed to determine the pathophysiology and different symptoms of the disease. |
doi_str_mv | 10.1016/j.ijscr.2023.108580 |
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A 21-year-old female came to our hospital complaining of tachycardia, high temperature, and tumor formation in the frontal region with a fistula. The examination of the thyroid gland and other systems was normal. The radiological investigations showed a severe lytic osseous lesion with aggressive destruction of the bone. The ultrasound imaging of the thyroid gland revealed that the thyroid was generally hypoechoic and heterogeneous because of many small hypoechoic focuses. In addition, the blood perfusion increased in the gland. The laboratory investigations were within normal expect C-reactive protein, free T4, and TSH. The surgery was indicated. The patient underwent an excision of the mass by a specialist in neurosurgery. The histopathological examination of the excised mass revealed LCH (eosinophilic granuloma). After 6 months, the patient underwent cranioplasty. The follow-up was uneventful for 3 months until the patient suffered from hyperthyroidism.
LCH can form in any part of the body, and cause many symptoms depending on its location. Even though hyperthyroidism is a rare and unexpected symptom of LCH.
LCH is a disease with broad-spectrum manifestations, so it should be a differential diagnosis in bone, thyroid, skin, and other organ lesions. In addition, thyroid ultrasonography and laboratory investigations are important methods to estimate thyroid functions and determine the clinical classification of the disease.
•LCH is a disease with broad-spectrum manifestations, so it should be a differential diagnosis in bone, thyroid, skin, and other organ lesions.•Thyroid ultrasonography and laboratory investigations are important methods to estimate thyroid functions and determine the clinical classification of the disease.•More studies are needed to determine the pathophysiology and different symptoms of the disease.</description><identifier>ISSN: 2210-2612</identifier><identifier>EISSN: 2210-2612</identifier><identifier>DOI: 10.1016/j.ijscr.2023.108580</identifier><identifier>PMID: 37531878</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>A case report ; Case Report ; Frontal bone ; Hyperthyroidism ; Langerhans cell histiocytosis</subject><ispartof>International journal of surgery case reports, 2023-08, Vol.109, p.108580, Article 108580</ispartof><rights>2023</rights><rights>Copyright © 2023 The Authors. Published by Elsevier Ltd.. All rights reserved.</rights><rights>2023 The Authors 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c427t-e254c4f160c25938d7c567e64f1a798392ce16fdbcc43ac9c548c987ab3b2f8b3</citedby><cites>FETCH-LOGICAL-c427t-e254c4f160c25938d7c567e64f1a798392ce16fdbcc43ac9c548c987ab3b2f8b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10415687/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ijscr.2023.108580$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,3550,27924,27925,45995,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37531878$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tawashi, Kenana</creatorcontrib><creatorcontrib>Khattab, Karam</creatorcontrib><title>Langerhans cell histiocytosis of the frontal bone with unexpected manifestations: Rare case report</title><title>International journal of surgery case reports</title><addtitle>Int J Surg Case Rep</addtitle><description>Langerhans cell histiocytosis (LCH) is a disease caused by clonal expansion of myeloid precursors that differentiate into specialized dendritic cells.
A 21-year-old female came to our hospital complaining of tachycardia, high temperature, and tumor formation in the frontal region with a fistula. The examination of the thyroid gland and other systems was normal. The radiological investigations showed a severe lytic osseous lesion with aggressive destruction of the bone. The ultrasound imaging of the thyroid gland revealed that the thyroid was generally hypoechoic and heterogeneous because of many small hypoechoic focuses. In addition, the blood perfusion increased in the gland. The laboratory investigations were within normal expect C-reactive protein, free T4, and TSH. The surgery was indicated. The patient underwent an excision of the mass by a specialist in neurosurgery. The histopathological examination of the excised mass revealed LCH (eosinophilic granuloma). After 6 months, the patient underwent cranioplasty. The follow-up was uneventful for 3 months until the patient suffered from hyperthyroidism.
LCH can form in any part of the body, and cause many symptoms depending on its location. Even though hyperthyroidism is a rare and unexpected symptom of LCH.
LCH is a disease with broad-spectrum manifestations, so it should be a differential diagnosis in bone, thyroid, skin, and other organ lesions. In addition, thyroid ultrasonography and laboratory investigations are important methods to estimate thyroid functions and determine the clinical classification of the disease.
•LCH is a disease with broad-spectrum manifestations, so it should be a differential diagnosis in bone, thyroid, skin, and other organ lesions.•Thyroid ultrasonography and laboratory investigations are important methods to estimate thyroid functions and determine the clinical classification of the disease.•More studies are needed to determine the pathophysiology and different symptoms of the disease.</description><subject>A case report</subject><subject>Case Report</subject><subject>Frontal bone</subject><subject>Hyperthyroidism</subject><subject>Langerhans cell histiocytosis</subject><issn>2210-2612</issn><issn>2210-2612</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kNtKBDEMhosoKuoTCNIX2LWHOXQEERFPsCCIXpdOJuN0mW2Xth727a2uit6Ym4Qk_x_yEXLI2ZQzXh3Pp3YeIUwFEzJ3VKnYBtkVgrOJqLjY_FXvkIMY5yyHFKoSYpvsyLqUXNVql7Qz454wDMZFCjiOdLAxWQ-r5KON1Pc0DUj74F0yI229Q_pq00CfHb4tERJ2dGGc7TEmk3UuntB7E5CCiUgDLn1I-2SrN2PEg6-8Rx6vLh8ubiazu-vbi_PZBApRpwmKsoCi5xUDUTZSdTWUVY1Vbpm6UbIRgLzquxagkAYaKAsFjapNK1vRq1bukbO17_K5XWAH6FIwo14GuzBhpb2x-u_E2UE_-RfNWcHLStXZQa4dIPgYA_Y_Ys70B3Y915_Y9Qd2vcaeVUe_7_5oviHnhdP1AubvXywGHcGiA-xsyAh15-2_B94BpzCXtg</recordid><startdate>20230801</startdate><enddate>20230801</enddate><creator>Tawashi, Kenana</creator><creator>Khattab, Karam</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope></search><sort><creationdate>20230801</creationdate><title>Langerhans cell histiocytosis of the frontal bone with unexpected manifestations: Rare case report</title><author>Tawashi, Kenana ; Khattab, Karam</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c427t-e254c4f160c25938d7c567e64f1a798392ce16fdbcc43ac9c548c987ab3b2f8b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>A case report</topic><topic>Case Report</topic><topic>Frontal bone</topic><topic>Hyperthyroidism</topic><topic>Langerhans cell histiocytosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tawashi, Kenana</creatorcontrib><creatorcontrib>Khattab, Karam</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International journal of surgery case reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tawashi, Kenana</au><au>Khattab, Karam</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Langerhans cell histiocytosis of the frontal bone with unexpected manifestations: Rare case report</atitle><jtitle>International journal of surgery case reports</jtitle><addtitle>Int J Surg Case Rep</addtitle><date>2023-08-01</date><risdate>2023</risdate><volume>109</volume><spage>108580</spage><pages>108580-</pages><artnum>108580</artnum><issn>2210-2612</issn><eissn>2210-2612</eissn><abstract>Langerhans cell histiocytosis (LCH) is a disease caused by clonal expansion of myeloid precursors that differentiate into specialized dendritic cells.
A 21-year-old female came to our hospital complaining of tachycardia, high temperature, and tumor formation in the frontal region with a fistula. The examination of the thyroid gland and other systems was normal. The radiological investigations showed a severe lytic osseous lesion with aggressive destruction of the bone. The ultrasound imaging of the thyroid gland revealed that the thyroid was generally hypoechoic and heterogeneous because of many small hypoechoic focuses. In addition, the blood perfusion increased in the gland. The laboratory investigations were within normal expect C-reactive protein, free T4, and TSH. The surgery was indicated. The patient underwent an excision of the mass by a specialist in neurosurgery. The histopathological examination of the excised mass revealed LCH (eosinophilic granuloma). After 6 months, the patient underwent cranioplasty. The follow-up was uneventful for 3 months until the patient suffered from hyperthyroidism.
LCH can form in any part of the body, and cause many symptoms depending on its location. Even though hyperthyroidism is a rare and unexpected symptom of LCH.
LCH is a disease with broad-spectrum manifestations, so it should be a differential diagnosis in bone, thyroid, skin, and other organ lesions. In addition, thyroid ultrasonography and laboratory investigations are important methods to estimate thyroid functions and determine the clinical classification of the disease.
•LCH is a disease with broad-spectrum manifestations, so it should be a differential diagnosis in bone, thyroid, skin, and other organ lesions.•Thyroid ultrasonography and laboratory investigations are important methods to estimate thyroid functions and determine the clinical classification of the disease.•More studies are needed to determine the pathophysiology and different symptoms of the disease.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>37531878</pmid><doi>10.1016/j.ijscr.2023.108580</doi><oa>free_for_read</oa></addata></record> |
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subjects | A case report Case Report Frontal bone Hyperthyroidism Langerhans cell histiocytosis |
title | Langerhans cell histiocytosis of the frontal bone with unexpected manifestations: Rare case report |
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