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Micropapillary mucinous adenocarcinoma of the lung: a brief case report. 肺微乳头状粘液腺癌1例报告。
Pub Date : 2013-12-01 Epub Date: 2013-12-24 DOI: 10.4132/KoreanJPathol.2013.47.6.603
In Ho Choi, Boin Lee, Joungho Han, Chin A Yi, Yong Soo Choi, Jin Seok Ahn
In 2011, the International Association for the Study of Lung Cancer/American Thoracic Society/European Respiratory Society (IASLC/ATS/ERS) classification added micropapillary predomi nant adenocarcinoma of the lung as a new histologic subtype and reclassified the former mucinous bronchioloalveolar carcino ma (BAC) as a variant of invasive mucinous adenocarcinoma. 1 Recent studies regarding epidermal growth factor receptor (EGFR) and K-ras mutations in lung cancer demonstrated that BAC with a lepidic or hobnail growth pattern is more typically associated with EGFR mutation, while mucinous differentiation is more common in cases with K-ras mutation. 2-4 However, these studies were based on the 2004 World Health Organization (WHO) classification, and there had been a few reports on the micropapillary pattern of this disease and its correlation with EGFR and K-ras mutations. 4,5 According to the report of the IASLC, 1 micropapillary predominant adenocarcinoma is known to be related to K-ras (33%), EGFR (20%), and BRAF (20%) mutations. Hypothesizing that micropapillary predominant adenocarcinoma with mucinous differentiation may be correlated with K-ras mutation, we performed a histological review of a case of micropapillary mucinous adenocarcinoma with associated K-ras mutation.
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引用次数: 2
Myxoid solitary fibrous tumor of the central nervous system. 中枢神经系统粘液样孤立性纤维性肿瘤。
Pub Date : 2013-12-01 Epub Date: 2013-12-24 DOI: 10.4132/KoreanJPathol.2013.47.6.505
Haeri Han, Sangjeong Ahn, Won Hwangbo, Yang Seok Chae
Solitary fibrous tumors (SFTs) most commonly occur in the pleura, but may also occur in the central nervous system (CNS). Among the numerous cases of CNS SFT that have been reported, totaling to more than 220 cases, the myxoid SFT of the CNS has been the least recognized and most misleading subtype.1 Differential diagnosis from chordoid or myxo-chordoid meningioma, myxoid peripheral nerve sheath tumor, metastatic or primary low-grade fibromyxoid sarcoma, primary intracranial myxoma, and metastatic tumor from a cardiac primary tumor is therefore necessary. Here, we present a case of a myxoid SFT located in the tentorium cerebelli. A 45-year-old woman presented with headache, general weakness, and impaired vision. A magnetic resonance imaging scan revealed a lunulating, contoured, enhancing mass measuring 7.0×6.0×2.0 cm with hemorrhagic foci, located in the right posterior parietal and temporooccipital convexities. Under the diagnosis of meningioma, open craniotomy, right parietotemporooccipital, and subtotal tumor removal was performed. Upon observation, many firm, rubbery, and bosselated tumor fragments, tan-white in color, were identified. The cut surface was relatively homogeneous, with a whitish fibrotic appearance and softer areas of gelatinous myxoid change, approximately 50%. Necrotic areas were not observed. Microscopic examination revealed a predominantly hypocellular area in the myxoid stroma, intervening with foci of a morphologically typical, densely cellular SFT with spindle cells and collagenous stroma (Fig. 1). In the hypocellular and myxoid areas, a proliferation of cytologically bland spindled cells was randomly arranged in a loose myxoid matrix, forming interconnecting strands, and resulting in degeneration. The neoplastic cells had oval to elongated nuclei, with evenly distributed chromatin, inconspicuous nucleoli, and scant pale cytoplasm. Immunohistochemically, the tumor cells showed a strong expression of CD34, vimentin, Bcl2 and CD99, but were negative for epithelial membrane antigen (EMA), pan-cytokeratin, and glial fibrillary acidic protein (GFAP). The Ki-67 labeling index was lower than 4%. On the basis of these findings, the final diagnosis was myxoid SFT. Fig. 1 Histologic findings. Myxoid stroma with focal ropy collagen in a rich vascularized tumor (A), moderately cellular area exhibiting spindle cells and collagenous stroma (B), and strong immunoreactivity for CD34 (C). Myxoid SFT of the CNS is an extremely rare tumor and differential diagnosis may be difficult to achieve owing to confusion with several other myxoid spindle cell neoplasms. Indeed, myxoid SFT of the CNS must be differentiated from chordoid or myxo-chordoid meningioma, myxoid peripheral nerve sheath tumor, metastatic or primary low-grade fibromyxoid sarcoma, primary intracranial myxoma, meningeal hemangiopericytoma and metastatic tumor from a cardiac primary. Immunohistochemistry has proven to be a useful tool in attaining an accu
{"title":"Myxoid solitary fibrous tumor of the central nervous system.","authors":"Haeri Han, Sangjeong Ahn, Won Hwangbo, Yang Seok Chae","doi":"10.4132/KoreanJPathol.2013.47.6.505","DOIUrl":"https://doi.org/10.4132/KoreanJPathol.2013.47.6.505","url":null,"abstract":"Solitary fibrous tumors (SFTs) most commonly occur in the pleura, but may also occur in the central nervous system (CNS). Among the numerous cases of CNS SFT that have been reported, totaling to more than 220 cases, the myxoid SFT of the CNS has been the least recognized and most misleading subtype.1 Differential diagnosis from chordoid or myxo-chordoid meningioma, myxoid peripheral nerve sheath tumor, metastatic or primary low-grade fibromyxoid sarcoma, primary intracranial myxoma, and metastatic tumor from a cardiac primary tumor is therefore necessary. Here, we present a case of a myxoid SFT located in the tentorium cerebelli. A 45-year-old woman presented with headache, general weakness, and impaired vision. A magnetic resonance imaging scan revealed a lunulating, contoured, enhancing mass measuring 7.0×6.0×2.0 cm with hemorrhagic foci, located in the right posterior parietal and temporooccipital convexities. Under the diagnosis of meningioma, open craniotomy, right parietotemporooccipital, and subtotal tumor removal was performed. \u0000 \u0000Upon observation, many firm, rubbery, and bosselated tumor fragments, tan-white in color, were identified. The cut surface was relatively homogeneous, with a whitish fibrotic appearance and softer areas of gelatinous myxoid change, approximately 50%. Necrotic areas were not observed. Microscopic examination revealed a predominantly hypocellular area in the myxoid stroma, intervening with foci of a morphologically typical, densely cellular SFT with spindle cells and collagenous stroma (Fig. 1). In the hypocellular and myxoid areas, a proliferation of cytologically bland spindled cells was randomly arranged in a loose myxoid matrix, forming interconnecting strands, and resulting in degeneration. The neoplastic cells had oval to elongated nuclei, with evenly distributed chromatin, inconspicuous nucleoli, and scant pale cytoplasm. Immunohistochemically, the tumor cells showed a strong expression of CD34, vimentin, Bcl2 and CD99, but were negative for epithelial membrane antigen (EMA), pan-cytokeratin, and glial fibrillary acidic protein (GFAP). The Ki-67 labeling index was lower than 4%. On the basis of these findings, the final diagnosis was myxoid SFT. \u0000 \u0000 \u0000 \u0000Fig. 1 \u0000 \u0000Histologic findings. Myxoid stroma with focal ropy collagen in a rich vascularized tumor (A), moderately cellular area exhibiting spindle cells and collagenous stroma (B), and strong immunoreactivity for CD34 (C). \u0000 \u0000 \u0000 \u0000Myxoid SFT of the CNS is an extremely rare tumor and differential diagnosis may be difficult to achieve owing to confusion with several other myxoid spindle cell neoplasms. Indeed, myxoid SFT of the CNS must be differentiated from chordoid or myxo-chordoid meningioma, myxoid peripheral nerve sheath tumor, metastatic or primary low-grade fibromyxoid sarcoma, primary intracranial myxoma, meningeal hemangiopericytoma and metastatic tumor from a cardiac primary. \u0000 \u0000Immunohistochemistry has proven to be a useful tool in attaining an accu","PeriodicalId":49936,"journal":{"name":"Korean Journal of Pathology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2013-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4132/KoreanJPathol.2013.47.6.505","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32027553","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Microtubule-Associated Protein Tau, α-Tubulin and βIII-Tubulin Expression in Breast Cancer. 微管相关蛋白Tau、α-微管蛋白和β iii -微管蛋白在乳腺癌中的表达。
Pub Date : 2013-12-01 Epub Date: 2013-12-24 DOI: 10.4132/KoreanJPathol.2013.47.6.534
Soyoung Im, Changyoung Yoo, Ji-Han Jung, Ye-Won Jeon, Young Jin Suh, Youn Soo Lee, Hyun Joo Choi

Background: The microtubule-associated protein Tau binds to both inner and outer surfaces of microtubules, leading to tubulin assembly and microtubule stabilization. The aim of this study was to evaluate the significance of Tau, α-tubulin, and βIII-tubulin expression in breast carcinoma and to assess their relationships with disease progression in the context of taxane treatment.

Methods: Immunohistochemical expressions of Tau, α-tubulin, and βIII-tubulin were assessed in 183 breast cancer cases. Expression was correlated with clinicopathologic parameters, disease progression and overall survival.

Results: Tau expression was correlated with lymph node metastasis and estrogen receptor (ER) positivity (p=.003 and p<.001, respectively). Loss of α-tubulin was significantly correlated with distant metastasis (p=.034). Loss of βIII-tubulin was correlated with lymph node metastasis and ER positivity (p=.004 and p<.001, respectively). In taxane-treated cases, Tau expression and loss of α-tubulin and βIII-tubulin expression were related to disease progression (p=.001, p=.028, and p=.030, respectively). Tau expression was associated with a worse survival rate in taxane-treated patients (p=.049).

Conclusions: Tau expression and loss of α-tubulin and βIII-tubulin expression were correlated with aggressive behavior in taxane-treated breast cancer. Further evaluation of Tau, α-tubulin and βIII-tubulin may be useful in predicting clinical behavior and seeking therapeutic measures in taxane-based chemotherapy for breast cancer.

背景:微管相关蛋白Tau结合到微管的内外表面,导致微管蛋白组装和微管稳定。本研究的目的是评估乳腺癌中Tau、α-微管蛋白和β iii -微管蛋白表达的意义,并评估它们在紫杉烷治疗背景下与疾病进展的关系。方法:对183例乳腺癌患者进行Tau、α-微管蛋白、β iii微管蛋白的免疫组化表达测定。表达与临床病理参数、疾病进展和总生存期相关。结果:Tau表达与淋巴结转移及雌激素受体(ER)阳性相关(p=。结论:紫杉烷治疗乳腺癌中Tau蛋白表达、α-微管蛋白和β iii微管蛋白表达缺失与侵袭行为相关。进一步评估Tau、α-微管蛋白和β iii -微管蛋白可能有助于预测乳腺癌紫杉烷化疗的临床行为和寻求治疗措施。
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引用次数: 7
Immunohistochemical classification of primary and secondary glioblastomas. 原发性和继发性胶质母细胞瘤的免疫组织化学分类。
Pub Date : 2013-12-01 Epub Date: 2013-12-24 DOI: 10.4132/KoreanJPathol.2013.47.6.541
Kyu Sang Lee, Gheeyoung Choe, Kyung Han Nam, An Na Seo, Sumi Yun, Kyung Ju Kim, Hwa Jin Cho, Sung Hye Park

Background: Glioblastomas may develop de novo (primary glioblastomas, P-GBLs) or through progression from lower-grade astrocytomas (secondary glioblastomas, S-GBLs). The aim of this study was to compare the immunohistochemical classification of glioblastomas with clinically determined P-GBLs and S-GBLs to identify the best combination of antibodies for immunohistochemical classification.

Methods: We evaluated the immunohistochemical expression of epidermal growth factor receptor (EGFR), p53, and isocitrate dehydrogenase 1 (IDH-1) in 150 glioblastoma cases.

Results: According to clinical history, the glioblastomas analyzed in this study consisted of 146 P-GBLs and 4 S-GBLs. Immunohistochemical expression of EGFR, p53, and IDH-1 was observed in 62.6%, 49.3%, and 11.1%, respectively. Immunohistochemical profiles of EGFR(+)/p53(-), IDH-1(-)/EGFR(+)/p53(-), and EGFR(-)/p53(+) were noted in 41.3%, 40.2%, and 28.7%, respectively. Expression of IDH-1 and EGFR(-)/p53(+) was positively correlated with young age. The typical immunohistochemical features of S-GBLs comprised IDH-1(+)/EGFR(-)/p53(+), and were noted in 3.6% of clinically P-GBLs. The combination of IDH-1(-) or EGFR(+) was the best set of immunohistochemical stains for identifying P-GBLs, whereas the combination of IDH-1(+) and EGFR(-) was best for identifying S-GBLs.

Conclusions: We recommend a combination of IDH-1 and EGFR for immunohistochemical classification of glioblastomas. We expect our results to be useful for determining treatment strategies for glioblastoma patients.

背景:胶质母细胞瘤可能会发展为新生(原发性胶质母细胞瘤,P-GBLs)或通过低级别星形细胞瘤(继发性胶质母细胞瘤,S-GBLs)发展而来。本研究的目的是比较胶质母细胞瘤的免疫组织化学分类与临床确定的P-GBLs和S-GBLs,以确定免疫组织化学分类的最佳抗体组合。方法:研究150例胶质母细胞瘤患者表皮生长因子受体(EGFR)、p53和异柠檬酸脱氢酶1 (IDH-1)的免疫组化表达。结果:根据临床病史,本研究分析的胶质母细胞瘤包括146例p - gbl和4例s - gbl。EGFR、p53和IDH-1的免疫组化表达分别为62.6%、49.3%和11.1%。EGFR(+)/p53(-)、IDH-1(-)/EGFR(+)/p53(-)和EGFR(-)/p53(+)的免疫组化谱分别为41.3%、40.2%和28.7%。IDH-1和EGFR(-)/p53(+)的表达与年龄呈正相关。S-GBLs的典型免疫组织化学特征包括IDH-1(+)/EGFR(-)/p53(+),在3.6%的临床P-GBLs中发现。IDH-1(-)或EGFR(+)组合是鉴定p - gbl的最佳免疫组化染色组,而IDH-1(+)和EGFR(-)组合是鉴定s - gbl的最佳免疫组化染色组。结论:我们推荐将IDH-1和EGFR联合用于胶质母细胞瘤的免疫组织化学分类。我们希望我们的结果对确定胶质母细胞瘤患者的治疗策略有用。
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引用次数: 24
Endogenous gastric-resident mesenchymal stem cells contribute to formation of cancer stroma and progression of gastric cancer. 内源性胃间充质干细胞参与胃癌间质形成和进展。
Pub Date : 2013-12-01 Epub Date: 2013-12-24 DOI: 10.4132/KoreanJPathol.2013.47.6.507
Eun-Kyung Kim, Hye-Jung Kim, Young-Il Yang, Jong Tae Kim, Min-Young Choi, Chang Soo Choi, Kwang-Hee Kim, Jeong-Han Lee, Won-Hee Jang, Soon-Ho Cheong

Background: Carcinoma-associated fibroblasts (CAFs) contribute to carcinogenesis and cancer progression, although their origin and role remain unclear. We recently identified and investigated the in situ identity and implications of gastric submucosa-resident mesenchymal stem cells (GS-MSCs) in the progression of gastric carcinogenesis.

Methods: We isolated GS-MSCs from gastric submucosa using hydrogel-supported organ culture and defined their identity. Isolated cells were assessed in vitro by immunophenotype and mesengenic multipotency. Reciprocal interactions between GS-MSCs and gastric cancer cells were evaluated. To determine the role of GS-MSCs, xenografts were constructed of gastric cancer cells admixed with or without GS-MSCs.

Results: Isolated cells fulfilled MSCs requirements in regard to plastic adherence, stromal cell immunophenotype, and multipotency. We demonstrated a paracrine loop that gastric cancer cells enhanced the migration, proliferation, and differentiation of GS-MSCs; additionally, GS-MSCs promoted the proliferation of gastric cancer cell in vitro. Xenograft experiments showed that GS-MSCs significantly promoted cancer growth and angiogenesis. GS-MSCs that integrated into gastric cancer became not only CAFs but also rarely endothelial cells which contributed to the formation of cellular and vascular cancer stroma.

Conclusions: Endogenous GS-MSCs play an important role in gastric cancer progression.

背景:癌相关成纤维细胞(CAFs)参与癌变和癌症进展,尽管其起源和作用尚不清楚。我们最近发现并研究了胃粘膜下间充质干细胞(GS-MSCs)在胃癌发生过程中的原位鉴定及其意义。方法:采用水凝胶支持的器官培养方法从胃粘膜下层分离GS-MSCs,并对其进行鉴定。通过免疫表型和间生多能性对分离细胞进行体外评价。研究了GS-MSCs与胃癌细胞之间的相互作用。为了确定GS-MSCs的作用,我们将胃癌细胞混合或不混合GS-MSCs构建异种移植物。结果:分离的细胞在可塑性粘附、基质细胞免疫表型和多能性方面满足MSCs的要求。我们证明了一个旁分泌环,胃癌细胞增强了GS-MSCs的迁移、增殖和分化;此外,GS-MSCs还能促进胃癌细胞的体外增殖。异种移植实验表明,GS-MSCs显著促进肿瘤生长和血管生成。整合到胃癌中的GS-MSCs不仅成为caf,而且很少成为内皮细胞,内皮细胞有助于细胞和血管癌基质的形成。结论:内源性GS-MSCs在胃癌进展中起重要作用。
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引用次数: 12
Diffuse Large B-Cell Lymphoma Arising in Warthin's Tumor: Case Study and Review of the Literature. 弥漫性大b细胞淋巴瘤发生于沃辛氏瘤:个案研究及文献回顾。
Pub Date : 2013-12-01 Epub Date: 2013-12-24 DOI: 10.4132/KoreanJPathol.2013.47.6.579
Güliz Ozkök, Funda Taşlı, Nazan Ozsan, Rafet Oztürk, Hakan Postacı

Warthin's tumor is the second most common type of salivary gland tumor. Microscopically, Warthin's tumor displays a proliferative epithelial component and lymphoid stroma. Carcinomas arising from the epithelial component are well known, but malignant transformations of the lymphoid stroma are rare. When they do occur, they are most commonly B-cell type non-Hodgkin lymphomas. A 60-year-old male patient underwent surgical resection of a parotid mass. After superficial parotidectomy, microscopic examination indicated that the tumor was of epithelial components with basaloid and oncocytic columns of cells neighboring lymphoid components. In addition to the lymphoid follicles with distinct germinal centers, there were large, bizarre and extremely atypical neoplastic cells seen in the lymphoid component. Large neoplastic cells were diffusely CD20 and CD30 positive. The patient was diagnosed with "Warthin's tumor and diffuse large B-cell lymphoma with expression of CD30." The histopathologic and clinical features are discussed along with a review of the literature.

沃辛氏肿瘤是第二常见的唾液腺肿瘤。显微镜下,Warthin肿瘤显示增生上皮成分和淋巴样基质。由上皮成分引起的癌是众所周知的,但淋巴样基质的恶性转化是罕见的。当它们确实发生时,它们最常见的是b细胞型非霍奇金淋巴瘤。一位六十岁男性病患接受手术切除腮腺肿物。腮腺浅表切除术后,镜检显示肿瘤为上皮成分,基底细胞和嗜瘤细胞柱邻近淋巴成分。淋巴滤泡除有明显的生发中心外,淋巴成分中还可见巨大的、奇异的、极不典型的肿瘤细胞。大肿瘤细胞弥漫性CD20和CD30阳性。患者被诊断为“伴有CD30表达的Warthin肿瘤和弥漫性大b细胞淋巴瘤”。组织病理学和临床特征进行讨论,并回顾文献。
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引用次数: 15
Diagnostic Accuracy of Cerebrospinal Fluid (CSF) Cytology in Metastatic Tumors: An Analysis of Consecutive CSF Samples. 脑脊液细胞学诊断转移性肿瘤的准确性:连续脑脊液样本的分析。
Pub Date : 2013-12-01 Epub Date: 2013-12-24 DOI: 10.4132/KoreanJPathol.2013.47.6.563
Yoon Sung Bae, June-Won Cheong, Won Seok Chang, Sewha Kim, Eun Ji Oh, Se Hoon Kim

Background: Cerebrospinal fluid (CSF) examination can be used to verify the presence of primary malignancies as well as cases of central nervous system (CNS) metastasis. Because of its importance, there have been several studies concerning the sensitivity of CSF cytology. To determine the practical use and reproducibility of diagnoses based on CSF cytology, we evaluated this test by analyzing cytology results from consecutive CSF samples.

Methods: Between July 2010 and June 2013, 385 CSF cytology samples from 42 patients were collected. The samples were gathered using a ventricular catheter and reservoir. CSF cytology of all patients was examined more than two times with immunocytochemistry for cytokeratin.

Results: Primary neoplastic sites and histologic types of patients' metastatic cancer were diverse. The overall sensitivity for detecting malignancy was 41.3%. Even within short-term intervals, diagnoses frequently changed.

Conclusions: Our results were inconsistent, with low sensitivity, when compared to the results of previous studies. However, CSF evaluation can still provide valuable diagnostic and prognostic information because adjuvant treatments are now routinely performed in patients with CNS metastasis. Negative CSF cytology results should not be ignored, and continuous CSF follow-up is essential for following the clinical course of patients with metastatic cancer involving the CNS.

背景:脑脊液(CSF)检查可用于证实原发性恶性肿瘤的存在以及中枢神经系统(CNS)转移的病例。由于脑脊液细胞学的重要性,已有一些关于脑脊液细胞学敏感性的研究。为了确定基于脑脊液细胞学诊断的实际用途和可重复性,我们通过分析连续脑脊液样本的细胞学结果来评估该测试。方法:2010年7月至2013年6月收集42例患者的脑脊液细胞学样本385份。使用心室导管和贮液器收集样本。所有患者的脑脊液细胞学检查超过两次,免疫细胞化学检测细胞角蛋白。结果:转移癌原发部位和组织学类型多样。检测恶性肿瘤的总体敏感性为41.3%。即使在短期内,诊断也经常发生变化。结论:与以往的研究结果相比,我们的结果不一致,灵敏度低。然而,脑脊液评估仍然可以提供有价值的诊断和预后信息,因为辅助治疗现在通常用于中枢神经系统转移患者。脑脊液细胞学阴性结果不应被忽视,持续的脑脊液随访对于追踪累及中枢神经系统的转移性癌症患者的临床病程至关重要。
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引用次数: 10
Cystic benign phyllodes tumor in the inguinal region. 腹股沟区囊性良性叶状瘤。
Pub Date : 2013-12-01 Epub Date: 2013-12-24 DOI: 10.4132/KoreanJPathol.2013.47.6.583
Jai Hyang Go

The present lesion was the first reported case of a benign intracystic phyllodes tumor in the inguinal region. We report the case of a 51-year-old female patient who presented with an inguinal mass. A clinical diagnosis of malignant lymphoma was considered in this case. The resected tumor was well-circumscribed and showed numerous papillary nodular protrusions into a central cystic cavity (3.5×2.5 cm). The microscopic findings showed hyperplastic epithelium-lined cysts with leaf-like intraluminal epithelium-lined bland stromal projections. The epithelial cell linings were strongly positive for estrogen and progesterone receptors.

本病例为腹股沟区良性囊内叶状瘤的首例报告病例。我们报告的情况下,51岁的女性患者谁提出腹股沟肿块。本病例临床诊断为恶性淋巴瘤。切除的肿瘤边界清晰,可见大量乳头状结节状突起进入中央囊腔(3.5×2.5 cm)。镜下可见增生性上皮细胞壁囊肿伴叶状腔内上皮细胞壁淡色间质突起。上皮细胞内雌激素和孕激素受体呈强阳性。
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引用次数: 2
Mediastinal thymolipoma with striated myoid cells: report of a peculiar case. 纵膈胸腺脂肪瘤伴横纹肌样细胞:一例特殊病例报告。
Pub Date : 2013-12-01 Epub Date: 2013-12-24 DOI: 10.4132/KoreanJPathol.2013.47.6.596
Young Keum Kim, Nari Shin, Won Young Park, Do Youn Park, Gi Young Huh, Chang Hun Lee
Thymolipoma is a rare anterior mediastinal tumor composed of mature adipose tissue and benign thymic tissue, and is a benign neoplasm for which complete surgical excision is curative.1 Literature has reported that the thymic parenchyma of thymolipoma exceptionally contain myoid cells that are immunoreactive for desmin, muscle-specific actin and myoglobin.2,3 Herein, we describe a very rare case of thymolipoma with myoid cells. To the best of our knowledge, this is the sixth case of thymolipoma containing striated myoid cells in the English literature since 1972.
{"title":"Mediastinal thymolipoma with striated myoid cells: report of a peculiar case.","authors":"Young Keum Kim,&nbsp;Nari Shin,&nbsp;Won Young Park,&nbsp;Do Youn Park,&nbsp;Gi Young Huh,&nbsp;Chang Hun Lee","doi":"10.4132/KoreanJPathol.2013.47.6.596","DOIUrl":"https://doi.org/10.4132/KoreanJPathol.2013.47.6.596","url":null,"abstract":"Thymolipoma is a rare anterior mediastinal tumor composed of mature adipose tissue and benign thymic tissue, and is a benign neoplasm for which complete surgical excision is curative.1 Literature has reported that the thymic parenchyma of thymolipoma exceptionally contain myoid cells that are immunoreactive for desmin, muscle-specific actin and myoglobin.2,3 Herein, we describe a very rare case of thymolipoma with myoid cells. To the best of our knowledge, this is the sixth case of thymolipoma containing striated myoid cells in the English literature since 1972.","PeriodicalId":49936,"journal":{"name":"Korean Journal of Pathology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2013-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4132/KoreanJPathol.2013.47.6.596","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32028642","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
Inflammatory Pseudotumor-like Follicular Dendritic Cell Tumor of the Spleen with Extensive Histiocytic Granulomas and Necrosis: A Case Report and Literature Review. 脾脏炎性假瘤样滤泡树突状细胞瘤伴广泛组织细胞肉芽肿和坏死1例报告并文献复习。
Pub Date : 2013-12-01 Epub Date: 2013-12-24 DOI: 10.4132/KoreanJPathol.2013.47.6.599
Hyun-Jung Kim, Ji Eun Kim, Gu-Hyun Kang, Jung Yeon Kim, Kyeongmee Park
Inflammatory pseudotumor (IPT)-like follicular dendritic cell tumor (FDCT) has been recently designated1 and characterized by proliferation of Epstein-Barr virus (EBV)-positive follicular dendritic cell (FDC) and commonly occurs in the liver and spleen.2-9 Histologically, it is characterized by spindle cell proliferation admixed with abundant inflammatory cells, mainly lymphocytes and plasma cells. At present, the preferred term 'inflammatory myofibroblastic tumor' is used, because it has been shown that the proliferating spindle cells show a myofibroblastic phenotype in many cases.1 About 20 cases have been reported,2,9 although only one case has been reported in Korea.9 We present here a rare case of IPT-like FDCT of the spleen with extensive histiocytic granulomas and necrosis, including a brief literature review.
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引用次数: 9
期刊
Korean Journal of Pathology
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