BACKGROUND Primary sebaceous carcinoma of lacrimal gland(SCLG) is extremely rare. Due to its clinical characteristics, it is often misdiagnosed. It is known to be aggressive so delay in diagnosis can increase the chan...BACKGROUND Primary sebaceous carcinoma of lacrimal gland(SCLG) is extremely rare. Due to its clinical characteristics, it is often misdiagnosed. It is known to be aggressive so delay in diagnosis can increase the chance of local recurrence and metastasis. We report a case of primary SCLG.CASE SUMMARY A 75-year-old man was referred with a painful swelling in the right eyelid. Computed tomography scan demonstrates a 2.6 cm mass in upper outer quadrant of right orbit. After the incisional biopsy of the mass, he was diagnosed with squamous cell carcinoma of lacrimal gland. A right orbital exenteration, cervical lymph node dissection was performed. There was no involvement of the overlying periorbital skin, eyelid, or conjunctiva. Histological examination of the exenteration specimen showed tumor arising from the lacrimal gland, which had been entirely replaced by sebaceous carcinoma with sarcomatous and squamous differentiation. Neoplastic cells which were large and contained prominent nucleoli. Focal tumor remained in the posterior resection margin. Patient underwent adjuvant radiotherapy, total dose of 56 Gy with doseper-fraction 2 Gy to primary lesion. There has been no sign of recurrence until 2-years follow-up.CONCLUSION We report a rare case of sebaceous carcinoma arising from the lacrimal gland. Accurate diagnosis of SCLG is important for appropriate treatment and prognosis prediction.展开更多
We investigated the sebaceous gland metaplasia(SGM) of the esophagus and clarified the evidence of misdiagnosis and its diagnosis pitfall. Cases of pathologically proven SGM were enrolled in the clinical analysis and ...We investigated the sebaceous gland metaplasia(SGM) of the esophagus and clarified the evidence of misdiagnosis and its diagnosis pitfall. Cases of pathologically proven SGM were enrolled in the clinical analysis and reviewed description of endoscope. In the current study, we demonstrated that SGM is very rare esophageal condition with an incidence around 0.00465% and an occurrence rate of 0.41 per year. There were 57.1% of senior endoscopists identified 8 episodes of SGM. In contrast, 7.7% of junior endoscopists identified SGM in only 2 episodes. Moreover, we investigated the difference in endoscopic biopsy attempt rate between the senior and junior endoscopist(P = 0.0001). The senior endoscopists had more motivation to look for SGM than did junior endoscopists(P = 0.01). We concluded that SGM of the esophagus is rare condition that is easily and not recognized in endoscopy studies omitting pathological review.展开更多
The antimicrobial properties of cis-6-hexadecenoic acid (C16:1Δ6), a component of the innate human metabolome, were studied and its application to cosmetic products was investigated in detail. A variety of the reside...The antimicrobial properties of cis-6-hexadecenoic acid (C16:1Δ6), a component of the innate human metabolome, were studied and its application to cosmetic products was investigated in detail. A variety of the resident and transient microbial flora of the skin, oral cavity, and intestine was applied to an investigation of the antimicrobial activity of C16:1Δ6. C16:1Δ6 showed selective antibacterial activity against human microbial pathogens such as Clostridium perfringens (one of the most common causes of food poisoning) and Streptococcus mutans (one of the tooth-decaying bacteria), as well as Staphylococcus aureus. C16:1Δ6 seemed to possess a “species-selective” antibacterial activity against bacteria belonging to the genera Staphylococcus and Clostridium. We performed a preliminary assessment of the application of C16:1Δ6 as an antimicrobial component in a liquid lip gloss by performing preservation efficacy and home-use tests. We noted that the amount of p-hydroxybenzoate was needed in an oily cosmetic, especially liquid lip gloss, could be reduced by replacing p-hydroxybenzoate with C16:1Δ6. We suggest that C16:1Δ6 may find application as a stable antimicrobial substance gentle enough for use in consumer products by its selective antimicrobial characteristics.展开更多
Background In humans telomerase is expressed in most ca ncers and immortal cell lines, and astivation of telomerase may play important r oles in tumorigenesis and immortalization. This study was to investigate the rol...Background In humans telomerase is expressed in most ca ncers and immortal cell lines, and astivation of telomerase may play important r oles in tumorigenesis and immortalization. This study was to investigate the rol es of telomerase activity (TA) and human telomerase RNA (hTR) in sebaceous carcinoma of the eyelid.Methods The telomerase repeated amplification protocal (TRAP) was used to demonstrate telomerase activity in 12 cases of sebaceous carcinoma of the eyelid. In situ hybridiza tion (ISH) was used to demonstrate the expression of hTR in 55 cases of paraffin-embedded sebaceous carcinoma of the eyelid, and the results were compared with the proliferative index determined by Mib-1 immuno-labeling, histological patterns and r ecurrence of the tumor.Results Different telomerase activity was shown in the 12 cases of sebaceous carcinoma of the eyelid. The positive expression of hTR was 85.5% (47/55) in tumor cells, but not in the adjacent tissues. The positive expression of hTR was correlated with the proliferative activity (as assessed by Mib-1 immunolabelling, r=0.942, P<0.001) and the dif ferentiation of sebaceous carcinoma of the eyelid (χ 2=17.621, P<0.001), but not si gnificantly related to tumor recurrence. The level of hTR expression increased with the de crease of differentiation of sebaceous carcinoma of the eyelid.Conclusions The results suggest that the up-regulation of telo merase expression plays some roles in tarsal gland carcinogenesis, and the express ion of hTR is a useful marker for malignant degree of sebaceous carcinoma of the eyelid.展开更多
BACKGROUND Sebaceous carcinoma(SC),a malignancy primarily characterized by aggressive growth,affects cutaneous tissues of the periocular region.Extraocular SC is extremely rare,especially in the extremities,as evidenc...BACKGROUND Sebaceous carcinoma(SC),a malignancy primarily characterized by aggressive growth,affects cutaneous tissues of the periocular region.Extraocular SC is extremely rare,especially in the extremities,as evidenced by only a handful of reported cases.CASE SUMMARY A 65-year-old man presented with a rapidly enlarging swelling on the left inner thigh,which was initially misdiagnosed as a subcutaneous abscess.The lesion had appeared two months prior to admission.Clinical examination revealed a cauliflower-like swollen content,with an ulcerated and infected mass located on his left thigh.At the same time,we observed solitary nodular lesions in his lungs and brain,with biopsy pathology of the lung lesions found to be consistent with the mass in the thigh.The patient received chemotherapy comprising cis-platinum with fluorouracil,followed by targeted therapy with anlotinib hydrochloride and chemotherapy with vinorelbine,implantation of iodine-125 seeds in the thigh and pulmonary tumor.The initial stage intervention achieved partial remission.The efficacy of maintenance treatment was evaluated as stable disease after the first 5 cycles;however,the patient developed a new brain lesion after the sixth cycle of treatment,which resulted in progressive disease and he received whole brain gamma knife radiotherapy.CONCLUSION We analyzed the clinical presentation,imaging features,pathology and treatment of a rare case of lung,brain and lymph node metastasis of SC located in the thigh.It is evident that cis-platinum combined with fluorouracil,vinorelbine combined with anlotinib hydrochloride may be an effective therapeutic regimen in advanced SC.However,brain metastatic lesions should receive early radiotherapy.展开更多
Introduction:Trichofolliculoma characterized clinically by the presence of acentral dilated pore with tufted hairs and corresponds histologically to a central primary follicle and many secondary vellus hair follicles ...Introduction:Trichofolliculoma characterized clinically by the presence of acentral dilated pore with tufted hairs and corresponds histologically to a central primary follicle and many secondary vellus hair follicles originating from it.Thus far,dermoscopy dascription of trichofolliculoma has been lacking.Here,we describe a typical case of trichofolliculoma,particularly the special manifestation under the dermoscopy.Case presentation:A 29-year-old man complained a five-year history of a nodule containing a central whitish hair plug on his left tempus.Dermoscopic examination revealed a well-defined,yellow macule with a central whitish hair plug surrounded by dilated capillaries,and histopathological analysis was consistent with trichofolliculoma.Discussion:The findings of dermoscopy were also vary,which may be affected by the origin of the disease,various phases of the hair cycle,depth of the lesion,and even external stimulus.Conclusion:Diagnosis of trichofolliculoma is sometimes difficult because the presence of the central crater and visible hairs is low,and dermoscopy examination may be a potentially useful diagnostic tool.展开更多
Sebaceous carcinoma (SC) of the eyelid is a rare but aggressive malignancy, accounting for 3%—5% of eyelid malignancies in the United States, and up to 35% in Asian populations (Deprez and Uffer, 2009;Xu et al., 2018...Sebaceous carcinoma (SC) of the eyelid is a rare but aggressive malignancy, accounting for 3%—5% of eyelid malignancies in the United States, and up to 35% in Asian populations (Deprez and Uffer, 2009;Xu et al., 2018;Yu et al., 2018). It is frequently mistaken for benign conditions or less aggressive malignancies such as basal cell carcinoma (Muqit et al., 2013), and the effects of delay in diagnosis can be devastating to patients. Aggressive surgical resection is the primary treatment of these tumors and often invoIves orbital exenteration with significant morbidity to patients, and these tumors frequently recur, with local recurrence rate as high as 18%. Importantly, this disease has a high metastatic potential, and there are very limited data guiding systemic treatment options;ultimately 6%—18% of patients diagnosed with SC of the eyelid succumb to metastatic disease (Zurcher et al., 1998;Shields et al., 2004).展开更多
Introduction:Muir-Torre syndrome is a phenotypic variant of Lynch syndrome characterized by a predisposition for the development of visceral malignant disease and sebaceous gland neoplasms,and it is caused by germline...Introduction:Muir-Torre syndrome is a phenotypic variant of Lynch syndrome characterized by a predisposition for the development of visceral malignant disease and sebaceous gland neoplasms,and it is caused by germline mutations in the mismatch repair genesMSH2 andMLH1.Case presentation:The proband was a 42-year-old man who had undergone surgical resection of colorectal adenocarcinoma at 28 years.He presented with macular rashes and red papule.Histological examination of the lesion on his head revealed a sebaceoma at 37 years.Follow-up of the family history revealed that the proband’s 65-year-old mother had been highly suspected to have Lynch syndrome with colorectal cancer at 40 years of age.The proband’s daughter underwent colonoscopy because of blood in the stool at the age of 13 years,but no abnormalities were found.Discussion:We have herein reported a pathogenic missense mutation c.199G>A(p.Gly67Arg)in exon 2 ofMLH1 in patients with MTS.This mutation has been reported in patients with Lynch syndrome who have no skin tumors.However,we also found that some patients with MTS had no history of any internal malignancy or skin tumor.Our data support the idea that a hiatus of many years may pass before both elements-a sebaceous neoplasm and an internal cancer-are present in a patient,thus finally allowing the diagnosis of MTS.Conclusion:A pathogenic Lynch syndrome mutation c.199G>A in exon 2 of theMLH1 gene was found in a patient with MTS who presented with a sebaceous neoplasm.展开更多
BACKGROUND Sebaceous lymphadenoma is a benign tumor that occurs rarely in the salivary glands,most commonly in the parotid glands or periparotid lymph nodes,and even more rarely undergoes malignant transformation into...BACKGROUND Sebaceous lymphadenoma is a benign tumor that occurs rarely in the salivary glands,most commonly in the parotid glands or periparotid lymph nodes,and even more rarely undergoes malignant transformation into a sebaceous lymphadenocarcinoma.CASE SUMMARY We report an 82-year-old woman who presented with a painless mass in the right parotid region.We performed extended surgical resection of the parotid gland mass.Intraoperative pathology revealed a sebaceous lymphadenocarcinoma with metastasis into the periparotid cervical lymph nodes,so we also performed neck dissection and lymph node resection.Postoperative pathology confirmed the diagnosis.The literature review revealed that this was the seventh reported case of sebaceous lymphadenocarcinoma and the second reported case of cervical lymph node metastasis and infiltration of the skin of the parotid gland.CONCLUSION Treatment of sebaceous lymphadenocarcinoma depends on the typing and clinical staging of the cancer.Extensive resection is the first choice,and adjuvant radiotherapy should be given to patients with high-grade tumors or those at an advanced clinical stage.展开更多
Introduction Nevus sebaceous (NS), also known as nevus sebaceous of Jadassohn, is a congenital sebaceous hyperplasia or organoid nevus. This benign congenital hamartoma is composed of abnormal epidermal and dermal com...Introduction Nevus sebaceous (NS), also known as nevus sebaceous of Jadassohn, is a congenital sebaceous hyperplasia or organoid nevus. This benign congenital hamartoma is composed of abnormal epidermal and dermal com-ponents. The hamartomatous lesions, usually clinically present at birth, are most frequently distributed on areas with sebaceous glands, especially the scalp and face(1)NS originates from pluripotent primordial epithelial germ tissue and occurs in approximately 0.1%of newborns.展开更多
文摘BACKGROUND Primary sebaceous carcinoma of lacrimal gland(SCLG) is extremely rare. Due to its clinical characteristics, it is often misdiagnosed. It is known to be aggressive so delay in diagnosis can increase the chance of local recurrence and metastasis. We report a case of primary SCLG.CASE SUMMARY A 75-year-old man was referred with a painful swelling in the right eyelid. Computed tomography scan demonstrates a 2.6 cm mass in upper outer quadrant of right orbit. After the incisional biopsy of the mass, he was diagnosed with squamous cell carcinoma of lacrimal gland. A right orbital exenteration, cervical lymph node dissection was performed. There was no involvement of the overlying periorbital skin, eyelid, or conjunctiva. Histological examination of the exenteration specimen showed tumor arising from the lacrimal gland, which had been entirely replaced by sebaceous carcinoma with sarcomatous and squamous differentiation. Neoplastic cells which were large and contained prominent nucleoli. Focal tumor remained in the posterior resection margin. Patient underwent adjuvant radiotherapy, total dose of 56 Gy with doseper-fraction 2 Gy to primary lesion. There has been no sign of recurrence until 2-years follow-up.CONCLUSION We report a rare case of sebaceous carcinoma arising from the lacrimal gland. Accurate diagnosis of SCLG is important for appropriate treatment and prognosis prediction.
文摘We investigated the sebaceous gland metaplasia(SGM) of the esophagus and clarified the evidence of misdiagnosis and its diagnosis pitfall. Cases of pathologically proven SGM were enrolled in the clinical analysis and reviewed description of endoscope. In the current study, we demonstrated that SGM is very rare esophageal condition with an incidence around 0.00465% and an occurrence rate of 0.41 per year. There were 57.1% of senior endoscopists identified 8 episodes of SGM. In contrast, 7.7% of junior endoscopists identified SGM in only 2 episodes. Moreover, we investigated the difference in endoscopic biopsy attempt rate between the senior and junior endoscopist(P = 0.0001). The senior endoscopists had more motivation to look for SGM than did junior endoscopists(P = 0.01). We concluded that SGM of the esophagus is rare condition that is easily and not recognized in endoscopy studies omitting pathological review.
文摘The antimicrobial properties of cis-6-hexadecenoic acid (C16:1Δ6), a component of the innate human metabolome, were studied and its application to cosmetic products was investigated in detail. A variety of the resident and transient microbial flora of the skin, oral cavity, and intestine was applied to an investigation of the antimicrobial activity of C16:1Δ6. C16:1Δ6 showed selective antibacterial activity against human microbial pathogens such as Clostridium perfringens (one of the most common causes of food poisoning) and Streptococcus mutans (one of the tooth-decaying bacteria), as well as Staphylococcus aureus. C16:1Δ6 seemed to possess a “species-selective” antibacterial activity against bacteria belonging to the genera Staphylococcus and Clostridium. We performed a preliminary assessment of the application of C16:1Δ6 as an antimicrobial component in a liquid lip gloss by performing preservation efficacy and home-use tests. We noted that the amount of p-hydroxybenzoate was needed in an oily cosmetic, especially liquid lip gloss, could be reduced by replacing p-hydroxybenzoate with C16:1Δ6. We suggest that C16:1Δ6 may find application as a stable antimicrobial substance gentle enough for use in consumer products by its selective antimicrobial characteristics.
文摘Background In humans telomerase is expressed in most ca ncers and immortal cell lines, and astivation of telomerase may play important r oles in tumorigenesis and immortalization. This study was to investigate the rol es of telomerase activity (TA) and human telomerase RNA (hTR) in sebaceous carcinoma of the eyelid.Methods The telomerase repeated amplification protocal (TRAP) was used to demonstrate telomerase activity in 12 cases of sebaceous carcinoma of the eyelid. In situ hybridiza tion (ISH) was used to demonstrate the expression of hTR in 55 cases of paraffin-embedded sebaceous carcinoma of the eyelid, and the results were compared with the proliferative index determined by Mib-1 immuno-labeling, histological patterns and r ecurrence of the tumor.Results Different telomerase activity was shown in the 12 cases of sebaceous carcinoma of the eyelid. The positive expression of hTR was 85.5% (47/55) in tumor cells, but not in the adjacent tissues. The positive expression of hTR was correlated with the proliferative activity (as assessed by Mib-1 immunolabelling, r=0.942, P<0.001) and the dif ferentiation of sebaceous carcinoma of the eyelid (χ 2=17.621, P<0.001), but not si gnificantly related to tumor recurrence. The level of hTR expression increased with the de crease of differentiation of sebaceous carcinoma of the eyelid.Conclusions The results suggest that the up-regulation of telo merase expression plays some roles in tarsal gland carcinogenesis, and the express ion of hTR is a useful marker for malignant degree of sebaceous carcinoma of the eyelid.
文摘BACKGROUND Sebaceous carcinoma(SC),a malignancy primarily characterized by aggressive growth,affects cutaneous tissues of the periocular region.Extraocular SC is extremely rare,especially in the extremities,as evidenced by only a handful of reported cases.CASE SUMMARY A 65-year-old man presented with a rapidly enlarging swelling on the left inner thigh,which was initially misdiagnosed as a subcutaneous abscess.The lesion had appeared two months prior to admission.Clinical examination revealed a cauliflower-like swollen content,with an ulcerated and infected mass located on his left thigh.At the same time,we observed solitary nodular lesions in his lungs and brain,with biopsy pathology of the lung lesions found to be consistent with the mass in the thigh.The patient received chemotherapy comprising cis-platinum with fluorouracil,followed by targeted therapy with anlotinib hydrochloride and chemotherapy with vinorelbine,implantation of iodine-125 seeds in the thigh and pulmonary tumor.The initial stage intervention achieved partial remission.The efficacy of maintenance treatment was evaluated as stable disease after the first 5 cycles;however,the patient developed a new brain lesion after the sixth cycle of treatment,which resulted in progressive disease and he received whole brain gamma knife radiotherapy.CONCLUSION We analyzed the clinical presentation,imaging features,pathology and treatment of a rare case of lung,brain and lymph node metastasis of SC located in the thigh.It is evident that cis-platinum combined with fluorouracil,vinorelbine combined with anlotinib hydrochloride may be an effective therapeutic regimen in advanced SC.However,brain metastatic lesions should receive early radiotherapy.
基金The study was supported by CAMS Innovation Fund for Medical Sciences(No.CIFMS-2017-I2M-1-017).
文摘Introduction:Trichofolliculoma characterized clinically by the presence of acentral dilated pore with tufted hairs and corresponds histologically to a central primary follicle and many secondary vellus hair follicles originating from it.Thus far,dermoscopy dascription of trichofolliculoma has been lacking.Here,we describe a typical case of trichofolliculoma,particularly the special manifestation under the dermoscopy.Case presentation:A 29-year-old man complained a five-year history of a nodule containing a central whitish hair plug on his left tempus.Dermoscopic examination revealed a well-defined,yellow macule with a central whitish hair plug surrounded by dilated capillaries,and histopathological analysis was consistent with trichofolliculoma.Discussion:The findings of dermoscopy were also vary,which may be affected by the origin of the disease,various phases of the hair cycle,depth of the lesion,and even external stimulus.Conclusion:Diagnosis of trichofolliculoma is sometimes difficult because the presence of the central crater and visible hairs is low,and dermoscopy examination may be a potentially useful diagnostic tool.
基金supported by the merge funding 2016e17, the Ninth People’s Hospital, Shanghai Jiao Tong University School of Medicinesupported by the Harrington Physician Scientist Pathway at University Hospitals Cleveland Medical Centerthe Clinical Translational Science Training Program TL1 grant at Case Western Reserve University
文摘Sebaceous carcinoma (SC) of the eyelid is a rare but aggressive malignancy, accounting for 3%—5% of eyelid malignancies in the United States, and up to 35% in Asian populations (Deprez and Uffer, 2009;Xu et al., 2018;Yu et al., 2018). It is frequently mistaken for benign conditions or less aggressive malignancies such as basal cell carcinoma (Muqit et al., 2013), and the effects of delay in diagnosis can be devastating to patients. Aggressive surgical resection is the primary treatment of these tumors and often invoIves orbital exenteration with significant morbidity to patients, and these tumors frequently recur, with local recurrence rate as high as 18%. Importantly, this disease has a high metastatic potential, and there are very limited data guiding systemic treatment options;ultimately 6%—18% of patients diagnosed with SC of the eyelid succumb to metastatic disease (Zurcher et al., 1998;Shields et al., 2004).
基金National Natural Science Foundation of China(Nos.31401071 and 81570960)。
文摘Introduction:Muir-Torre syndrome is a phenotypic variant of Lynch syndrome characterized by a predisposition for the development of visceral malignant disease and sebaceous gland neoplasms,and it is caused by germline mutations in the mismatch repair genesMSH2 andMLH1.Case presentation:The proband was a 42-year-old man who had undergone surgical resection of colorectal adenocarcinoma at 28 years.He presented with macular rashes and red papule.Histological examination of the lesion on his head revealed a sebaceoma at 37 years.Follow-up of the family history revealed that the proband’s 65-year-old mother had been highly suspected to have Lynch syndrome with colorectal cancer at 40 years of age.The proband’s daughter underwent colonoscopy because of blood in the stool at the age of 13 years,but no abnormalities were found.Discussion:We have herein reported a pathogenic missense mutation c.199G>A(p.Gly67Arg)in exon 2 ofMLH1 in patients with MTS.This mutation has been reported in patients with Lynch syndrome who have no skin tumors.However,we also found that some patients with MTS had no history of any internal malignancy or skin tumor.Our data support the idea that a hiatus of many years may pass before both elements-a sebaceous neoplasm and an internal cancer-are present in a patient,thus finally allowing the diagnosis of MTS.Conclusion:A pathogenic Lynch syndrome mutation c.199G>A in exon 2 of theMLH1 gene was found in a patient with MTS who presented with a sebaceous neoplasm.
文摘BACKGROUND Sebaceous lymphadenoma is a benign tumor that occurs rarely in the salivary glands,most commonly in the parotid glands or periparotid lymph nodes,and even more rarely undergoes malignant transformation into a sebaceous lymphadenocarcinoma.CASE SUMMARY We report an 82-year-old woman who presented with a painless mass in the right parotid region.We performed extended surgical resection of the parotid gland mass.Intraoperative pathology revealed a sebaceous lymphadenocarcinoma with metastasis into the periparotid cervical lymph nodes,so we also performed neck dissection and lymph node resection.Postoperative pathology confirmed the diagnosis.The literature review revealed that this was the seventh reported case of sebaceous lymphadenocarcinoma and the second reported case of cervical lymph node metastasis and infiltration of the skin of the parotid gland.CONCLUSION Treatment of sebaceous lymphadenocarcinoma depends on the typing and clinical staging of the cancer.Extensive resection is the first choice,and adjuvant radiotherapy should be given to patients with high-grade tumors or those at an advanced clinical stage.
基金the CAMS Innovation Fund for Medical Sciences(CIFMS-2017-I2M-1-017)the National Natural Science Foundation of China(81872216).
文摘Introduction Nevus sebaceous (NS), also known as nevus sebaceous of Jadassohn, is a congenital sebaceous hyperplasia or organoid nevus. This benign congenital hamartoma is composed of abnormal epidermal and dermal com-ponents. The hamartomatous lesions, usually clinically present at birth, are most frequently distributed on areas with sebaceous glands, especially the scalp and face(1)NS originates from pluripotent primordial epithelial germ tissue and occurs in approximately 0.1%of newborns.