A rare case report of pituicytoma with biphasic pattern and admixed with scattered Herring bodies
Pituicytoma is a rare pituitary non-neuroendocrine tumour. The awareness of pituitary non-neuroendocrine tumours has gradually increased over the past several decades, but the knowledge of some histological variants of the tumours is limited, particularly in clinicopathological significance. Here, w...
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Published in | World journal of surgical oncology Vol. 18; no. 1; p. 108 |
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Abstract | Pituicytoma is a rare pituitary non-neuroendocrine tumour. The awareness of pituitary non-neuroendocrine tumours has gradually increased over the past several decades, but the knowledge of some histological variants of the tumours is limited, particularly in clinicopathological significance. Here, we report a rare case of pituicytoma variant.
A 71-year-old man presented with sudden symptoms of stroke including urinary incontinence, weakness in right lower limb, and trouble speaking. Physical examinations showed a right facial paralysis. The radiological examinations eventually found a 1.7 × 1.4 × 1.3 cm sellar occupied lesion. After symptomatic treatment improved the symptoms, the patient underwent transsphenoidal resection of the pituitary mass. Histologically, the tumour contained hypocellular area and hypercellular area. The hypocellular area showed elongated spindle cells arranged in a fascicular pattern around small vessels and scattered Herring bodies; the hypercellular area showed a large number of pseudorosettes. Immunohistochemistrically, the tumour cells were positive for thyroid transcription factor-1, S100, and neuron-specific enolase. Neurofilament only showed a little positive in the hypocellular area, and silver impregnation was only noted in a perivascular distribution. The patient had no recurrence 4 months after the surgery.
The rare variant of pituicytoma has a favourable prognosis. Moreover, it needs to be distinguished pituicytomas with pseudorosettes from ependymomas because of different prognosis. Lastly, Herring bodies may occasionally be seen in the pituicytoma, which could be a potential diagnostic pitfall. |
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AbstractList | Pituicytoma is a rare pituitary non-neuroendocrine tumour. The awareness of pituitary non-neuroendocrine tumours has gradually increased over the past several decades, but the knowledge of some histological variants of the tumours is limited, particularly in clinicopathological significance. Here, we report a rare case of pituicytoma variant.
A 71-year-old man presented with sudden symptoms of stroke including urinary incontinence, weakness in right lower limb, and trouble speaking. Physical examinations showed a right facial paralysis. The radiological examinations eventually found a 1.7 × 1.4 × 1.3 cm sellar occupied lesion. After symptomatic treatment improved the symptoms, the patient underwent transsphenoidal resection of the pituitary mass. Histologically, the tumour contained hypocellular area and hypercellular area. The hypocellular area showed elongated spindle cells arranged in a fascicular pattern around small vessels and scattered Herring bodies; the hypercellular area showed a large number of pseudorosettes. Immunohistochemistrically, the tumour cells were positive for thyroid transcription factor-1, S100, and neuron-specific enolase. Neurofilament only showed a little positive in the hypocellular area, and silver impregnation was only noted in a perivascular distribution. The patient had no recurrence 4 months after the surgery.
The rare variant of pituicytoma has a favourable prognosis. Moreover, it needs to be distinguished pituicytomas with pseudorosettes from ependymomas because of different prognosis. Lastly, Herring bodies may occasionally be seen in the pituicytoma, which could be a potential diagnostic pitfall. Pituicytoma is a rare pituitary non-neuroendocrine tumour. The awareness of pituitary non-neuroendocrine tumours has gradually increased over the past several decades, but the knowledge of some histological variants of the tumours is limited, particularly in clinicopathological significance. Here, we report a rare case of pituicytoma variant. The rare variant of pituicytoma has a favourable prognosis. Moreover, it needs to be distinguished pituicytomas with pseudorosettes from ependymomas because of different prognosis. Lastly, Herring bodies may occasionally be seen in the pituicytoma, which could be a potential diagnostic pitfall. Background Pituicytoma is a rare pituitary non-neuroendocrine tumour. The awareness of pituitary non-neuroendocrine tumours has gradually increased over the past several decades, but the knowledge of some histological variants of the tumours is limited, particularly in clinicopathological significance. Here, we report a rare case of pituicytoma variant. Case presentation A 71-year-old man presented with sudden symptoms of stroke including urinary incontinence, weakness in right lower limb, and trouble speaking. Physical examinations showed a right facial paralysis. The radiological examinations eventually found a 1.7 x 1.4 x 1.3 cm sellar occupied lesion. After symptomatic treatment improved the symptoms, the patient underwent transsphenoidal resection of the pituitary mass. Histologically, the tumour contained hypocellular area and hypercellular area. The hypocellular area showed elongated spindle cells arranged in a fascicular pattern around small vessels and scattered Herring bodies; the hypercellular area showed a large number of pseudorosettes. Immunohistochemistrically, the tumour cells were positive for thyroid transcription factor-1, S100, and neuron-specific enolase. Neurofilament only showed a little positive in the hypocellular area, and silver impregnation was only noted in a perivascular distribution. The patient had no recurrence 4 months after the surgery. Conclusions The rare variant of pituicytoma has a favourable prognosis. Moreover, it needs to be distinguished pituicytomas with pseudorosettes from ependymomas because of different prognosis. Lastly, Herring bodies may occasionally be seen in the pituicytoma, which could be a potential diagnostic pitfall. Keywords: Pituicytoma, Perivascular pseudorosettes, TTF1, Pathology, Case report Abstract Background Pituicytoma is a rare pituitary non-neuroendocrine tumour. The awareness of pituitary non-neuroendocrine tumours has gradually increased over the past several decades, but the knowledge of some histological variants of the tumours is limited, particularly in clinicopathological significance. Here, we report a rare case of pituicytoma variant. Case presentation A 71-year-old man presented with sudden symptoms of stroke including urinary incontinence, weakness in right lower limb, and trouble speaking. Physical examinations showed a right facial paralysis. The radiological examinations eventually found a 1.7 × 1.4 × 1.3 cm sellar occupied lesion. After symptomatic treatment improved the symptoms, the patient underwent transsphenoidal resection of the pituitary mass. Histologically, the tumour contained hypocellular area and hypercellular area. The hypocellular area showed elongated spindle cells arranged in a fascicular pattern around small vessels and scattered Herring bodies; the hypercellular area showed a large number of pseudorosettes. Immunohistochemistrically, the tumour cells were positive for thyroid transcription factor-1, S100, and neuron-specific enolase. Neurofilament only showed a little positive in the hypocellular area, and silver impregnation was only noted in a perivascular distribution. The patient had no recurrence 4 months after the surgery. Conclusions The rare variant of pituicytoma has a favourable prognosis. Moreover, it needs to be distinguished pituicytomas with pseudorosettes from ependymomas because of different prognosis. Lastly, Herring bodies may occasionally be seen in the pituicytoma, which could be a potential diagnostic pitfall. Background Pituicytoma is a rare pituitary non-neuroendocrine tumour. The awareness of pituitary non-neuroendocrine tumours has gradually increased over the past several decades, but the knowledge of some histological variants of the tumours is limited, particularly in clinicopathological significance. Here, we report a rare case of pituicytoma variant. Case presentation A 71-year-old man presented with sudden symptoms of stroke including urinary incontinence, weakness in right lower limb, and trouble speaking. Physical examinations showed a right facial paralysis. The radiological examinations eventually found a 1.7 × 1.4 × 1.3 cm sellar occupied lesion. After symptomatic treatment improved the symptoms, the patient underwent transsphenoidal resection of the pituitary mass. Histologically, the tumour contained hypocellular area and hypercellular area. The hypocellular area showed elongated spindle cells arranged in a fascicular pattern around small vessels and scattered Herring bodies; the hypercellular area showed a large number of pseudorosettes. Immunohistochemistrically, the tumour cells were positive for thyroid transcription factor-1, S100, and neuron-specific enolase. Neurofilament only showed a little positive in the hypocellular area, and silver impregnation was only noted in a perivascular distribution. The patient had no recurrence 4 months after the surgery. Conclusions The rare variant of pituicytoma has a favourable prognosis. Moreover, it needs to be distinguished pituicytomas with pseudorosettes from ependymomas because of different prognosis. Lastly, Herring bodies may occasionally be seen in the pituicytoma, which could be a potential diagnostic pitfall. Abstract Background Pituicytoma is a rare pituitary non-neuroendocrine tumour. The awareness of pituitary non-neuroendocrine tumours has gradually increased over the past several decades, but the knowledge of some histological variants of the tumours is limited, particularly in clinicopathological significance. Here, we report a rare case of pituicytoma variant. Case presentation A 71-year-old man presented with sudden symptoms of stroke including urinary incontinence, weakness in right lower limb, and trouble speaking. Physical examinations showed a right facial paralysis. The radiological examinations eventually found a 1.7 × 1.4 × 1.3 cm sellar occupied lesion. After symptomatic treatment improved the symptoms, the patient underwent transsphenoidal resection of the pituitary mass. Histologically, the tumour contained hypocellular area and hypercellular area. The hypocellular area showed elongated spindle cells arranged in a fascicular pattern around small vessels and scattered Herring bodies; the hypercellular area showed a large number of pseudorosettes. Immunohistochemistrically, the tumour cells were positive for thyroid transcription factor-1, S100, and neuron-specific enolase. Neurofilament only showed a little positive in the hypocellular area, and silver impregnation was only noted in a perivascular distribution. The patient had no recurrence 4 months after the surgery. Conclusions The rare variant of pituicytoma has a favourable prognosis. Moreover, it needs to be distinguished pituicytomas with pseudorosettes from ependymomas because of different prognosis. Lastly, Herring bodies may occasionally be seen in the pituicytoma, which could be a potential diagnostic pitfall. BACKGROUNDPituicytoma is a rare pituitary non-neuroendocrine tumour. The awareness of pituitary non-neuroendocrine tumours has gradually increased over the past several decades, but the knowledge of some histological variants of the tumours is limited, particularly in clinicopathological significance. Here, we report a rare case of pituicytoma variant. CASE PRESENTATIONA 71-year-old man presented with sudden symptoms of stroke including urinary incontinence, weakness in right lower limb, and trouble speaking. Physical examinations showed a right facial paralysis. The radiological examinations eventually found a 1.7 × 1.4 × 1.3 cm sellar occupied lesion. After symptomatic treatment improved the symptoms, the patient underwent transsphenoidal resection of the pituitary mass. Histologically, the tumour contained hypocellular area and hypercellular area. The hypocellular area showed elongated spindle cells arranged in a fascicular pattern around small vessels and scattered Herring bodies; the hypercellular area showed a large number of pseudorosettes. Immunohistochemistrically, the tumour cells were positive for thyroid transcription factor-1, S100, and neuron-specific enolase. Neurofilament only showed a little positive in the hypocellular area, and silver impregnation was only noted in a perivascular distribution. The patient had no recurrence 4 months after the surgery. CONCLUSIONSThe rare variant of pituicytoma has a favourable prognosis. Moreover, it needs to be distinguished pituicytomas with pseudorosettes from ependymomas because of different prognosis. Lastly, Herring bodies may occasionally be seen in the pituicytoma, which could be a potential diagnostic pitfall. |
ArticleNumber | 108 |
Audience | Academic |
Author | Qin, Xue Zou, Lingfeng Tan, Yiwen Cao, Xiaojing Wang, Chenglong Zeng, Min Cao, Youde Zeng, Yan Wang, Lijuan |
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References | H Witt (1889_CR14) 2011; 20 EB Lee (1889_CR1) 2009; 68 R Gonzalez-Campora (1889_CR6) 1986; 57 DJ Brat (1889_CR16) 2000; 24 PJ Kurtin (1889_CR5) 1994; 25 T Yoshimoto (1889_CR10) 2015; 32 I Vajtai (1889_CR13) 2011; 122 BW Scheithauer (1889_CR9) 2009; 40 BH Le (1889_CR4) 2004; 128 AJ Ulm (1889_CR18) 2004; 54 A Sali (1889_CR8) 2017; 37 GW Ross (1889_CR15) 1989; 70 DA Chistiakov (1889_CR2) 2017; 97 Z Saeed Kamil (1889_CR11) 2014; 25 SM Karam (1889_CR7) 2003; 21 MJ Kwon (1889_CR12) 2011; 61 GZ Yang (1889_CR3) 2017; 25 H Takei (1889_CR17) 2005; 55 |
References_xml | – volume: 25 start-page: 436 issue: 4 year: 2014 ident: 1889_CR11 publication-title: Endocr Pathol doi: 10.1007/s12022-013-9279-2 contributor: fullname: Z Saeed Kamil – volume: 61 start-page: 598 issue: 10 year: 2011 ident: 1889_CR12 publication-title: Pathol Int doi: 10.1111/j.1440-1827.2011.02708.x contributor: fullname: MJ Kwon – volume: 21 start-page: 322 issue: 3 year: 2003 ident: 1889_CR7 publication-title: Stem Cells doi: 10.1634/stemcells.21-3-322 contributor: fullname: SM Karam – volume: 128 start-page: 771 issue: 7 year: 2004 ident: 1889_CR4 publication-title: Arch Pathol Lab Med doi: 10.5858/2004-128-771-GCTIAO contributor: fullname: BH Le – volume: 32 start-page: 221 issue: 3 year: 2015 ident: 1889_CR10 publication-title: Brain Tumor Pathol doi: 10.1007/s10014-015-0219-3 contributor: fullname: T Yoshimoto – volume: 122 start-page: 253 issue: 2 year: 2011 ident: 1889_CR13 publication-title: Acta Neuropathol doi: 10.1007/s00401-011-0835-x contributor: fullname: I Vajtai – volume: 57 start-page: 1154 issue: 6 year: 1986 ident: 1889_CR6 publication-title: Cancer doi: 10.1002/1097-0142(19860315)57:6<1154::AID-CNCR2820570616>3.0.CO;2-W contributor: fullname: R Gonzalez-Campora – volume: 37 start-page: 535 issue: 6 year: 2017 ident: 1889_CR8 publication-title: Neuropathology doi: 10.1111/neup.12393 contributor: fullname: A Sali – volume: 68 start-page: 482 issue: 5 year: 2009 ident: 1889_CR1 publication-title: J Neuropathol Exp Neurol doi: 10.1097/NEN.0b013e3181a13fca contributor: fullname: EB Lee – volume: 54 start-page: 753 issue: 3 year: 2004 ident: 1889_CR18 publication-title: Neurosurgery doi: 10.1227/01.NEU.0000108983.50966.B7 contributor: fullname: AJ Ulm – volume: 97 start-page: 4 issue: 1 year: 2017 ident: 1889_CR2 publication-title: Lab Invest doi: 10.1038/labinvest.2016.116 contributor: fullname: DA Chistiakov – volume: 24 start-page: 362 issue: 3 year: 2000 ident: 1889_CR16 publication-title: Am J Surg Pathol doi: 10.1097/00000478-200003000-00004 contributor: fullname: DJ Brat – volume: 25 start-page: 751 issue: 8 year: 2017 ident: 1889_CR3 publication-title: Int J Surg Pathol doi: 10.1177/1066896917712861 contributor: fullname: GZ Yang – volume: 70 start-page: 31 issue: 1 year: 1989 ident: 1889_CR15 publication-title: J Neurosurg doi: 10.3171/jns.1989.70.1.0031 contributor: fullname: GW Ross – volume: 25 start-page: 1172 issue: 11 year: 1994 ident: 1889_CR5 publication-title: Hum Pathol doi: 10.1016/0046-8177(94)90033-7 contributor: fullname: PJ Kurtin – volume: 55 start-page: 745 issue: 11 year: 2005 ident: 1889_CR17 publication-title: Pathol Int doi: 10.1111/j.1440-1827.2005.01890.x contributor: fullname: H Takei – volume: 40 start-page: 435 issue: 3 year: 2009 ident: 1889_CR9 publication-title: Hum Pathol doi: 10.1016/j.humpath.2008.08.013 contributor: fullname: BW Scheithauer – volume: 20 start-page: 143 issue: 2 year: 2011 ident: 1889_CR14 publication-title: Cancer Cell doi: 10.1016/j.ccr.2011.07.007 contributor: fullname: H Witt |
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Snippet | Pituicytoma is a rare pituitary non-neuroendocrine tumour. The awareness of pituitary non-neuroendocrine tumours has gradually increased over the past several... Abstract Background Pituicytoma is a rare pituitary non-neuroendocrine tumour. The awareness of pituitary non-neuroendocrine tumours has gradually increased... Background Pituicytoma is a rare pituitary non-neuroendocrine tumour. The awareness of pituitary non-neuroendocrine tumours has gradually increased over the... BACKGROUNDPituicytoma is a rare pituitary non-neuroendocrine tumour. The awareness of pituitary non-neuroendocrine tumours has gradually increased over the... Abstract Background Pituicytoma is a rare pituitary non-neuroendocrine tumour. The awareness of pituitary non-neuroendocrine tumours has gradually increased... |
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Title | A rare case report of pituicytoma with biphasic pattern and admixed with scattered Herring bodies |
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