A case of mantle cell lymphoma presenting as IgG4-related dacryoadenitis and sialoadenitis, so-called Mikulicz’s disease

Background Mantle cell lymphoma (MCL) is a relatively uncommon type of non-Hodgkin lymphoma. It develops in the outer edge of a lymph node called the mantle zone. In contrast, IgG4-related dacryoadenitis and sialoadenitis (IgG4-DS) is characterized by elevated serum IgG4 and persistent bilateral enl...
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Autor*in:	Hayashi, Yoshikazu [verfasserIn] Moriyama, Masafumi Maehara, Takashi Goto, Yuichi Kawano, Shintaro Ohta, Miho Tanaka, Akihiko Furukawa, Sachiko Hayashida, Jun-Nosuke Kiyoshima, Tamotsu Shimizu, Mayumi Chikui, Toru Nakamura, Seiji

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2015

Schlagwörter:	Mantle cell lymphoma IgG4-related dacryoadenitis and sialoadenitis Lacrimal glands Salivary glands

Anmerkung:	© Hayashi et al. 2015. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (

Übergeordnetes Werk:	Enthalten in: World journal of surgical oncology - London : Biomed Central, 2003, 13(2015), 1 vom: 25. Juli
Übergeordnetes Werk:	volume:13 ; year:2015 ; number:1 ; day:25 ; month:07

Links:	Volltext

DOI / URN:	10.1186/s12957-015-0644-0

Katalog-ID:	SPR028832159

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520			\|a Background Mantle cell lymphoma (MCL) is a relatively uncommon type of non-Hodgkin lymphoma. It develops in the outer edge of a lymph node called the mantle zone. In contrast, IgG4-related dacryoadenitis and sialoadenitis (IgG4-DS) is characterized by elevated serum IgG4 and persistent bilateral enlargement of lacrimal glands (LGs) and salivary glands (SGs), with infiltration of IgG4-positive plasma cells. Recent studies indicated the importance of differentiation between IgG4-DS and malignant lymphoma. Case presentation An 82-year-old man was suspected of IgG4-DS because of a high serum IgG level (2174 mg/dL) and bilateral swelling of LGs and SGs. Lip biopsy and fine needle biopsy of submandibular gland were performed, and subsequently, MCL was diagnosed through the histopathological findings. Conclusions MCL most commonly occurs in the Waldeyer ring, but rarely in the stomach, spleen, skin, LG, and SG. We report an unusual case of MCL involving LGs and SGs mimicking IgG4-DS, which suggests that IgG4 testing may be useful in the differentiation of IgG4-DS in the presence of bilateral swelling of LGs or SGs.
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allfields	10.1186/s12957-015-0644-0 doi (DE-627)SPR028832159 (SPR)s12957-015-0644-0-e DE-627 ger DE-627 rakwb eng Hayashi, Yoshikazu verfasserin aut A case of mantle cell lymphoma presenting as IgG4-related dacryoadenitis and sialoadenitis, so-called Mikulicz’s disease 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Hayashi et al. 2015. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( Background Mantle cell lymphoma (MCL) is a relatively uncommon type of non-Hodgkin lymphoma. It develops in the outer edge of a lymph node called the mantle zone. In contrast, IgG4-related dacryoadenitis and sialoadenitis (IgG4-DS) is characterized by elevated serum IgG4 and persistent bilateral enlargement of lacrimal glands (LGs) and salivary glands (SGs), with infiltration of IgG4-positive plasma cells. Recent studies indicated the importance of differentiation between IgG4-DS and malignant lymphoma. Case presentation An 82-year-old man was suspected of IgG4-DS because of a high serum IgG level (2174 mg/dL) and bilateral swelling of LGs and SGs. Lip biopsy and fine needle biopsy of submandibular gland were performed, and subsequently, MCL was diagnosed through the histopathological findings. Conclusions MCL most commonly occurs in the Waldeyer ring, but rarely in the stomach, spleen, skin, LG, and SG. We report an unusual case of MCL involving LGs and SGs mimicking IgG4-DS, which suggests that IgG4 testing may be useful in the differentiation of IgG4-DS in the presence of bilateral swelling of LGs or SGs. Mantle cell lymphoma (dpeaa)DE-He213 IgG4-related dacryoadenitis and sialoadenitis (dpeaa)DE-He213 Lacrimal glands (dpeaa)DE-He213 Salivary glands (dpeaa)DE-He213 Moriyama, Masafumi aut Maehara, Takashi aut Goto, Yuichi aut Kawano, Shintaro aut Ohta, Miho aut Tanaka, Akihiko aut Furukawa, Sachiko aut Hayashida, Jun-Nosuke aut Kiyoshima, Tamotsu aut Shimizu, Mayumi aut Chikui, Toru aut Nakamura, Seiji aut Enthalten in World journal of surgical oncology London : Biomed Central, 2003 13(2015), 1 vom: 25. Juli (DE-627)369082907 (DE-600)2118383-1 1477-7819 nnns volume:13 year:2015 number:1 day:25 month:07 https://dx.doi.org/10.1186/s12957-015-0644-0 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 13 2015 1 25 07
spelling	10.1186/s12957-015-0644-0 doi (DE-627)SPR028832159 (SPR)s12957-015-0644-0-e DE-627 ger DE-627 rakwb eng Hayashi, Yoshikazu verfasserin aut A case of mantle cell lymphoma presenting as IgG4-related dacryoadenitis and sialoadenitis, so-called Mikulicz’s disease 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Hayashi et al. 2015. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( Background Mantle cell lymphoma (MCL) is a relatively uncommon type of non-Hodgkin lymphoma. It develops in the outer edge of a lymph node called the mantle zone. In contrast, IgG4-related dacryoadenitis and sialoadenitis (IgG4-DS) is characterized by elevated serum IgG4 and persistent bilateral enlargement of lacrimal glands (LGs) and salivary glands (SGs), with infiltration of IgG4-positive plasma cells. Recent studies indicated the importance of differentiation between IgG4-DS and malignant lymphoma. Case presentation An 82-year-old man was suspected of IgG4-DS because of a high serum IgG level (2174 mg/dL) and bilateral swelling of LGs and SGs. Lip biopsy and fine needle biopsy of submandibular gland were performed, and subsequently, MCL was diagnosed through the histopathological findings. Conclusions MCL most commonly occurs in the Waldeyer ring, but rarely in the stomach, spleen, skin, LG, and SG. We report an unusual case of MCL involving LGs and SGs mimicking IgG4-DS, which suggests that IgG4 testing may be useful in the differentiation of IgG4-DS in the presence of bilateral swelling of LGs or SGs. Mantle cell lymphoma (dpeaa)DE-He213 IgG4-related dacryoadenitis and sialoadenitis (dpeaa)DE-He213 Lacrimal glands (dpeaa)DE-He213 Salivary glands (dpeaa)DE-He213 Moriyama, Masafumi aut Maehara, Takashi aut Goto, Yuichi aut Kawano, Shintaro aut Ohta, Miho aut Tanaka, Akihiko aut Furukawa, Sachiko aut Hayashida, Jun-Nosuke aut Kiyoshima, Tamotsu aut Shimizu, Mayumi aut Chikui, Toru aut Nakamura, Seiji aut Enthalten in World journal of surgical oncology London : Biomed Central, 2003 13(2015), 1 vom: 25. Juli (DE-627)369082907 (DE-600)2118383-1 1477-7819 nnns volume:13 year:2015 number:1 day:25 month:07 https://dx.doi.org/10.1186/s12957-015-0644-0 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 13 2015 1 25 07
allfields_unstemmed	10.1186/s12957-015-0644-0 doi (DE-627)SPR028832159 (SPR)s12957-015-0644-0-e DE-627 ger DE-627 rakwb eng Hayashi, Yoshikazu verfasserin aut A case of mantle cell lymphoma presenting as IgG4-related dacryoadenitis and sialoadenitis, so-called Mikulicz’s disease 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Hayashi et al. 2015. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( Background Mantle cell lymphoma (MCL) is a relatively uncommon type of non-Hodgkin lymphoma. It develops in the outer edge of a lymph node called the mantle zone. In contrast, IgG4-related dacryoadenitis and sialoadenitis (IgG4-DS) is characterized by elevated serum IgG4 and persistent bilateral enlargement of lacrimal glands (LGs) and salivary glands (SGs), with infiltration of IgG4-positive plasma cells. Recent studies indicated the importance of differentiation between IgG4-DS and malignant lymphoma. Case presentation An 82-year-old man was suspected of IgG4-DS because of a high serum IgG level (2174 mg/dL) and bilateral swelling of LGs and SGs. Lip biopsy and fine needle biopsy of submandibular gland were performed, and subsequently, MCL was diagnosed through the histopathological findings. Conclusions MCL most commonly occurs in the Waldeyer ring, but rarely in the stomach, spleen, skin, LG, and SG. We report an unusual case of MCL involving LGs and SGs mimicking IgG4-DS, which suggests that IgG4 testing may be useful in the differentiation of IgG4-DS in the presence of bilateral swelling of LGs or SGs. Mantle cell lymphoma (dpeaa)DE-He213 IgG4-related dacryoadenitis and sialoadenitis (dpeaa)DE-He213 Lacrimal glands (dpeaa)DE-He213 Salivary glands (dpeaa)DE-He213 Moriyama, Masafumi aut Maehara, Takashi aut Goto, Yuichi aut Kawano, Shintaro aut Ohta, Miho aut Tanaka, Akihiko aut Furukawa, Sachiko aut Hayashida, Jun-Nosuke aut Kiyoshima, Tamotsu aut Shimizu, Mayumi aut Chikui, Toru aut Nakamura, Seiji aut Enthalten in World journal of surgical oncology London : Biomed Central, 2003 13(2015), 1 vom: 25. Juli (DE-627)369082907 (DE-600)2118383-1 1477-7819 nnns volume:13 year:2015 number:1 day:25 month:07 https://dx.doi.org/10.1186/s12957-015-0644-0 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 13 2015 1 25 07
allfieldsGer	10.1186/s12957-015-0644-0 doi (DE-627)SPR028832159 (SPR)s12957-015-0644-0-e DE-627 ger DE-627 rakwb eng Hayashi, Yoshikazu verfasserin aut A case of mantle cell lymphoma presenting as IgG4-related dacryoadenitis and sialoadenitis, so-called Mikulicz’s disease 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Hayashi et al. 2015. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( Background Mantle cell lymphoma (MCL) is a relatively uncommon type of non-Hodgkin lymphoma. It develops in the outer edge of a lymph node called the mantle zone. In contrast, IgG4-related dacryoadenitis and sialoadenitis (IgG4-DS) is characterized by elevated serum IgG4 and persistent bilateral enlargement of lacrimal glands (LGs) and salivary glands (SGs), with infiltration of IgG4-positive plasma cells. Recent studies indicated the importance of differentiation between IgG4-DS and malignant lymphoma. Case presentation An 82-year-old man was suspected of IgG4-DS because of a high serum IgG level (2174 mg/dL) and bilateral swelling of LGs and SGs. Lip biopsy and fine needle biopsy of submandibular gland were performed, and subsequently, MCL was diagnosed through the histopathological findings. Conclusions MCL most commonly occurs in the Waldeyer ring, but rarely in the stomach, spleen, skin, LG, and SG. We report an unusual case of MCL involving LGs and SGs mimicking IgG4-DS, which suggests that IgG4 testing may be useful in the differentiation of IgG4-DS in the presence of bilateral swelling of LGs or SGs. Mantle cell lymphoma (dpeaa)DE-He213 IgG4-related dacryoadenitis and sialoadenitis (dpeaa)DE-He213 Lacrimal glands (dpeaa)DE-He213 Salivary glands (dpeaa)DE-He213 Moriyama, Masafumi aut Maehara, Takashi aut Goto, Yuichi aut Kawano, Shintaro aut Ohta, Miho aut Tanaka, Akihiko aut Furukawa, Sachiko aut Hayashida, Jun-Nosuke aut Kiyoshima, Tamotsu aut Shimizu, Mayumi aut Chikui, Toru aut Nakamura, Seiji aut Enthalten in World journal of surgical oncology London : Biomed Central, 2003 13(2015), 1 vom: 25. Juli (DE-627)369082907 (DE-600)2118383-1 1477-7819 nnns volume:13 year:2015 number:1 day:25 month:07 https://dx.doi.org/10.1186/s12957-015-0644-0 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 13 2015 1 25 07
allfieldsSound	10.1186/s12957-015-0644-0 doi (DE-627)SPR028832159 (SPR)s12957-015-0644-0-e DE-627 ger DE-627 rakwb eng Hayashi, Yoshikazu verfasserin aut A case of mantle cell lymphoma presenting as IgG4-related dacryoadenitis and sialoadenitis, so-called Mikulicz’s disease 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Hayashi et al. 2015. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( Background Mantle cell lymphoma (MCL) is a relatively uncommon type of non-Hodgkin lymphoma. It develops in the outer edge of a lymph node called the mantle zone. In contrast, IgG4-related dacryoadenitis and sialoadenitis (IgG4-DS) is characterized by elevated serum IgG4 and persistent bilateral enlargement of lacrimal glands (LGs) and salivary glands (SGs), with infiltration of IgG4-positive plasma cells. Recent studies indicated the importance of differentiation between IgG4-DS and malignant lymphoma. Case presentation An 82-year-old man was suspected of IgG4-DS because of a high serum IgG level (2174 mg/dL) and bilateral swelling of LGs and SGs. Lip biopsy and fine needle biopsy of submandibular gland were performed, and subsequently, MCL was diagnosed through the histopathological findings. Conclusions MCL most commonly occurs in the Waldeyer ring, but rarely in the stomach, spleen, skin, LG, and SG. We report an unusual case of MCL involving LGs and SGs mimicking IgG4-DS, which suggests that IgG4 testing may be useful in the differentiation of IgG4-DS in the presence of bilateral swelling of LGs or SGs. Mantle cell lymphoma (dpeaa)DE-He213 IgG4-related dacryoadenitis and sialoadenitis (dpeaa)DE-He213 Lacrimal glands (dpeaa)DE-He213 Salivary glands (dpeaa)DE-He213 Moriyama, Masafumi aut Maehara, Takashi aut Goto, Yuichi aut Kawano, Shintaro aut Ohta, Miho aut Tanaka, Akihiko aut Furukawa, Sachiko aut Hayashida, Jun-Nosuke aut Kiyoshima, Tamotsu aut Shimizu, Mayumi aut Chikui, Toru aut Nakamura, Seiji aut Enthalten in World journal of surgical oncology London : Biomed Central, 2003 13(2015), 1 vom: 25. Juli (DE-627)369082907 (DE-600)2118383-1 1477-7819 nnns volume:13 year:2015 number:1 day:25 month:07 https://dx.doi.org/10.1186/s12957-015-0644-0 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 13 2015 1 25 07
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source	Enthalten in World journal of surgical oncology 13(2015), 1 vom: 25. Juli volume:13 year:2015 number:1 day:25 month:07
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This is an Open Access article distributed under the terms of the Creative Commons Attribution License (</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Background Mantle cell lymphoma (MCL) is a relatively uncommon type of non-Hodgkin lymphoma. It develops in the outer edge of a lymph node called the mantle zone. In contrast, IgG4-related dacryoadenitis and sialoadenitis (IgG4-DS) is characterized by elevated serum IgG4 and persistent bilateral enlargement of lacrimal glands (LGs) and salivary glands (SGs), with infiltration of IgG4-positive plasma cells. Recent studies indicated the importance of differentiation between IgG4-DS and malignant lymphoma. Case presentation An 82-year-old man was suspected of IgG4-DS because of a high serum IgG level (2174 mg/dL) and bilateral swelling of LGs and SGs. Lip biopsy and fine needle biopsy of submandibular gland were performed, and subsequently, MCL was diagnosed through the histopathological findings. Conclusions MCL most commonly occurs in the Waldeyer ring, but rarely in the stomach, spleen, skin, LG, and SG. 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author	Hayashi, Yoshikazu
spellingShingle	Hayashi, Yoshikazu misc Mantle cell lymphoma misc IgG4-related dacryoadenitis and sialoadenitis misc Lacrimal glands misc Salivary glands A case of mantle cell lymphoma presenting as IgG4-related dacryoadenitis and sialoadenitis, so-called Mikulicz’s disease
authorStr	Hayashi, Yoshikazu
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topic_title	A case of mantle cell lymphoma presenting as IgG4-related dacryoadenitis and sialoadenitis, so-called Mikulicz’s disease Mantle cell lymphoma (dpeaa)DE-He213 IgG4-related dacryoadenitis and sialoadenitis (dpeaa)DE-He213 Lacrimal glands (dpeaa)DE-He213 Salivary glands (dpeaa)DE-He213
topic	misc Mantle cell lymphoma misc IgG4-related dacryoadenitis and sialoadenitis misc Lacrimal glands misc Salivary glands
topic_unstemmed	misc Mantle cell lymphoma misc IgG4-related dacryoadenitis and sialoadenitis misc Lacrimal glands misc Salivary glands
topic_browse	misc Mantle cell lymphoma misc IgG4-related dacryoadenitis and sialoadenitis misc Lacrimal glands misc Salivary glands
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title	A case of mantle cell lymphoma presenting as IgG4-related dacryoadenitis and sialoadenitis, so-called Mikulicz’s disease
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title_full	A case of mantle cell lymphoma presenting as IgG4-related dacryoadenitis and sialoadenitis, so-called Mikulicz’s disease
author_sort	Hayashi, Yoshikazu
journal	World journal of surgical oncology
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author_browse	Hayashi, Yoshikazu Moriyama, Masafumi Maehara, Takashi Goto, Yuichi Kawano, Shintaro Ohta, Miho Tanaka, Akihiko Furukawa, Sachiko Hayashida, Jun-Nosuke Kiyoshima, Tamotsu Shimizu, Mayumi Chikui, Toru Nakamura, Seiji
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author-letter	Hayashi, Yoshikazu
doi_str_mv	10.1186/s12957-015-0644-0
title_sort	case of mantle cell lymphoma presenting as igg4-related dacryoadenitis and sialoadenitis, so-called mikulicz’s disease
title_auth	A case of mantle cell lymphoma presenting as IgG4-related dacryoadenitis and sialoadenitis, so-called Mikulicz’s disease
abstract	Background Mantle cell lymphoma (MCL) is a relatively uncommon type of non-Hodgkin lymphoma. It develops in the outer edge of a lymph node called the mantle zone. In contrast, IgG4-related dacryoadenitis and sialoadenitis (IgG4-DS) is characterized by elevated serum IgG4 and persistent bilateral enlargement of lacrimal glands (LGs) and salivary glands (SGs), with infiltration of IgG4-positive plasma cells. Recent studies indicated the importance of differentiation between IgG4-DS and malignant lymphoma. Case presentation An 82-year-old man was suspected of IgG4-DS because of a high serum IgG level (2174 mg/dL) and bilateral swelling of LGs and SGs. Lip biopsy and fine needle biopsy of submandibular gland were performed, and subsequently, MCL was diagnosed through the histopathological findings. Conclusions MCL most commonly occurs in the Waldeyer ring, but rarely in the stomach, spleen, skin, LG, and SG. We report an unusual case of MCL involving LGs and SGs mimicking IgG4-DS, which suggests that IgG4 testing may be useful in the differentiation of IgG4-DS in the presence of bilateral swelling of LGs or SGs. © Hayashi et al. 2015. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (
abstractGer	Background Mantle cell lymphoma (MCL) is a relatively uncommon type of non-Hodgkin lymphoma. It develops in the outer edge of a lymph node called the mantle zone. In contrast, IgG4-related dacryoadenitis and sialoadenitis (IgG4-DS) is characterized by elevated serum IgG4 and persistent bilateral enlargement of lacrimal glands (LGs) and salivary glands (SGs), with infiltration of IgG4-positive plasma cells. Recent studies indicated the importance of differentiation between IgG4-DS and malignant lymphoma. Case presentation An 82-year-old man was suspected of IgG4-DS because of a high serum IgG level (2174 mg/dL) and bilateral swelling of LGs and SGs. Lip biopsy and fine needle biopsy of submandibular gland were performed, and subsequently, MCL was diagnosed through the histopathological findings. Conclusions MCL most commonly occurs in the Waldeyer ring, but rarely in the stomach, spleen, skin, LG, and SG. We report an unusual case of MCL involving LGs and SGs mimicking IgG4-DS, which suggests that IgG4 testing may be useful in the differentiation of IgG4-DS in the presence of bilateral swelling of LGs or SGs. © Hayashi et al. 2015. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (
abstract_unstemmed	Background Mantle cell lymphoma (MCL) is a relatively uncommon type of non-Hodgkin lymphoma. It develops in the outer edge of a lymph node called the mantle zone. In contrast, IgG4-related dacryoadenitis and sialoadenitis (IgG4-DS) is characterized by elevated serum IgG4 and persistent bilateral enlargement of lacrimal glands (LGs) and salivary glands (SGs), with infiltration of IgG4-positive plasma cells. Recent studies indicated the importance of differentiation between IgG4-DS and malignant lymphoma. Case presentation An 82-year-old man was suspected of IgG4-DS because of a high serum IgG level (2174 mg/dL) and bilateral swelling of LGs and SGs. Lip biopsy and fine needle biopsy of submandibular gland were performed, and subsequently, MCL was diagnosed through the histopathological findings. Conclusions MCL most commonly occurs in the Waldeyer ring, but rarely in the stomach, spleen, skin, LG, and SG. We report an unusual case of MCL involving LGs and SGs mimicking IgG4-DS, which suggests that IgG4 testing may be useful in the differentiation of IgG4-DS in the presence of bilateral swelling of LGs or SGs. © Hayashi et al. 2015. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (
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title_short	A case of mantle cell lymphoma presenting as IgG4-related dacryoadenitis and sialoadenitis, so-called Mikulicz’s disease
url	https://dx.doi.org/10.1186/s12957-015-0644-0
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author2	Moriyama, Masafumi Maehara, Takashi Goto, Yuichi Kawano, Shintaro Ohta, Miho Tanaka, Akihiko Furukawa, Sachiko Hayashida, Jun-Nosuke Kiyoshima, Tamotsu Shimizu, Mayumi Chikui, Toru Nakamura, Seiji
author2Str	Moriyama, Masafumi Maehara, Takashi Goto, Yuichi Kawano, Shintaro Ohta, Miho Tanaka, Akihiko Furukawa, Sachiko Hayashida, Jun-Nosuke Kiyoshima, Tamotsu Shimizu, Mayumi Chikui, Toru Nakamura, Seiji
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up_date	2024-07-03T21:59:52.506Z
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This is an Open Access article distributed under the terms of the Creative Commons Attribution License (</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Background Mantle cell lymphoma (MCL) is a relatively uncommon type of non-Hodgkin lymphoma. It develops in the outer edge of a lymph node called the mantle zone. In contrast, IgG4-related dacryoadenitis and sialoadenitis (IgG4-DS) is characterized by elevated serum IgG4 and persistent bilateral enlargement of lacrimal glands (LGs) and salivary glands (SGs), with infiltration of IgG4-positive plasma cells. Recent studies indicated the importance of differentiation between IgG4-DS and malignant lymphoma. Case presentation An 82-year-old man was suspected of IgG4-DS because of a high serum IgG level (2174 mg/dL) and bilateral swelling of LGs and SGs. Lip biopsy and fine needle biopsy of submandibular gland were performed, and subsequently, MCL was diagnosed through the histopathological findings. Conclusions MCL most commonly occurs in the Waldeyer ring, but rarely in the stomach, spleen, skin, LG, and SG. We report an unusual case of MCL involving LGs and SGs mimicking IgG4-DS, which suggests that IgG4 testing may be useful in the differentiation of IgG4-DS in the presence of bilateral swelling of LGs or SGs.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Mantle cell lymphoma</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">IgG4-related dacryoadenitis and sialoadenitis</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Lacrimal glands</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Salivary glands</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Moriyama, Masafumi</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Maehara, Takashi</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Goto, Yuichi</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Kawano, Shintaro</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Ohta, Miho</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Tanaka, Akihiko</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Furukawa, Sachiko</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Hayashida, Jun-Nosuke</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Kiyoshima, Tamotsu</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Shimizu, Mayumi</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Chikui, Toru</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Nakamura, Seiji</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">World journal of surgical oncology</subfield><subfield code="d">London : Biomed Central, 2003</subfield><subfield code="g">13(2015), 1 vom: 25. 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A case of mantle cell lymphoma presenting as IgG4-related dacryoadenitis and sialoadenitis, so-called Mikulicz’s disease

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