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Simin

@SiminSh5

PGY-1 Resident | Volleyball player

เข้าร่วม Kasım 2022
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NotasDePatologia
NotasDePatologia@Notas_Patologia·
🔬 Serous Cystadenoma of the Pancreas: What You Need to Know Serous Cystadenoma of the Pancreas, also known as Microcystic Serous Adenoma, is a rare benign cystic neoplasm that shows a female predominance (3:1), typically diagnosed around the age of 58. It accounts for about one-third of primary pancreatic cysts. 🧬 In some cases, it may be associated with von Hippel-Lindau (VHL) syndrome, particularly when multifocal. 📍 Anatomical Location: Most frequently found in the tail of the pancreas, with a body/tail to head/neck ratio of about 1.6:1. In VHL-associated cases, it may involve the entire pancreas. 🔍 Gross Features: These are usually well-circumscribed lesions, averaging 6 cm in size but ranging from 1 to 30 cm. The most common type is microcystic, with a sponge-like appearance composed of numerous small cysts filled with clear fluid. Other types include: Oligocystic (Macrocystic): fewer, larger cysts Solid variant: homogeneous, gelatinous, and yellow-beige in appearance A classic feature is the presence of a central stellate scar, consisting of hyalinized fibrous tissue. Hemorrhage may occasionally occur. Multifocality is rare but more common in VHL patients. 🔬 Microscopic Findings: Cysts are lined by cuboidal to low columnar epithelium with clear cytoplasm rich in glycogen (PAS-positive, diastase-sensitive). Nuclei are round, uniform, with dense chromatin, inconspicuous nucleoli, and no mitoses. The stroma may range from edematous to fibrous, sometimes myxoid or hyalinized, and features a rich capillary network. Calcifications can be present. Variants include tiny papillary projections (without fibrovascular cores), oncocytic types with granular cytoplasm, and a solid variant with compact small glands and minimal lumina. 🧪 Immunohistochemistry: Tumor cells are typically positive for EMA, MUC1, pancytokeratin, inhibin, and GLUT1, and negative for HMB45. These markers help distinguish it from other cystic neoplasms. 🧬 Molecular and Cytogenetics: VHL gene alterations are common, especially in VHL patients, with loss of heterozygosity on chromosome 3p. Similar findings can occur in sporadic cases, suggesting a genetic component in tumorigenesis. 💧 Cyst Fluid Analysis: Fluid is typically low-viscosity, with low amylase and CEA (<5–20 ng/mL). Cytology shows cuboidal cells with glycogen-rich cytoplasm. In VHL patients, VHL gene mutations may be detected. 📈 Prognosis: This neoplasm is almost always benign, with slow growth (median 0.29 cm/year). The malignant transformation risk is <3%, and associated mortality is virtually nonexistent. Large tumors may compress adjacent organs but rarely pose significant clinical concern. 📌 Clinical-Pathologic Summary: Rare benign cystic neoplasm, mostly in middle-aged women Preferentially located in the pancreatic tail Characterized by clear fluid-filled microcysts and central scar Cuboidal epithelium with glycogen-rich cytoplasm and bland nuclei Immunopositive for EMA, MUC1, GLUT1 Associated with VHL gene alterations Excellent prognosis with minimal malignant potential 📚 References: Pathology Outlines – Serous cystadenoma StatPearls – Pancreatic Serous Cystadenoma Am J Surg Pathol 2015;39:1597 (PMID: 26559376) J Gastrointest Cancer 2010;41:197 (PMID: 20140653) Pancreatology 2009;9:182 (PMID: 19077470) Ultrastruct Pathol 2006;30:119 (PMID: 16517478) World J Surg 2003;27:319 (PMID: 12607059) Dig Surg 2016;33:240 (PMID: 26998825) Am J Pathol 2001;158:317 (PMID: 11141506) 📌 Disclaimer: This content is intended for healthcare professionals and is for educational and informational purposes only. It does not replace individualized clinical evaluation, medical judgment, or institutional guidelines. In real-world scenarios, specialist consultation and updated evidence-based protocols are essential. #SerousCystadenomaOfThePancreas #MedicalEducation #NotasDePatologia
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NotasDePatologia
NotasDePatologia@Notas_Patologia·
🔬Uterine Tuberculosis (UTB): An Under-recognized Cause of Infertility 🔬 What is it? Uterine tuberculosis (UTB) is the infection of the endometrium by Mycobacterium tuberculosis, usually via haematogenous spread from a pulmonary focus. It represents the most common form of female genital tuberculosis (FGTB), affecting the endometrium in ≈ 50–80 % of FGTB cases and causing infertility in 40–50 % of patients—especially in regions with a high TB burden such as India. Clinical Impact Typical profile: Women of reproductive age, often with primary infertility or long-standing menstrual disturbances (amenorrhoea, oligomenorrhoea, menorrhagia). Late sequelae: Intra-uterine adhesions (Asherman syndrome), reduced endometrial receptivity, increased risk of ectopic pregnancy (33–72 %). Only sporadic spontaneous pregnancies are reported after treatment. Assisted conception: IVF success rates vary widely (≈ 16–38 %), largely depending on endometrial integrity; baseline FSH tends to be higher and live-birth rates lower than in other infertility cohorts. Diagnostic Approach – Why It Is Challenging Imaging HSG: “Beaded” or “T-shaped” cavity, filling defects or “glove-finger” tube outline. Ultrasound/MRI: Heterogeneous or thin endometrium, intra-uterine synechiae, hydrosalpinx. Histopathology Endometrial biopsy/curettage (ideally late luteal phase): non-caseating or caseating granulomas with Langhans‐type giant cells. Sensitivity ≈ 50 % because menstrual shedding may remove granulomas. Bacteriology & Molecular tests AFB smear: low yield (< 10 %). Culture (L-J, MGIT): positive in 5–8 % of endometrial samples; takes weeks. PCR / GeneXpert MTB/RIF: high analytic sensitivity (< 10 bacilli mL⁻¹) and specificity but prone to false positives; GeneXpert data for FGTB still limited. LAMP assays: sensitivity ≈ 66 %. Endoscopy Hysteroscopy may reveal pale cavity, caseous nodules, “starry sky” tubercles, dense adhesions. Should be performed by experienced surgeons, often under laparoscopic control. Standard Therapy & Outcomes First-line regimen: 2 months HRZE → 4 months HR (isoniazid, rifampicin ± ethambutol). Clinical–microbiological cure rates reach ≈ 95 %. MDR-TB: 18–24 months with second-line agents; newer drugs (bedaquiline, delamanid) under evaluation for extrapulmonary disease. Follow-up: Endometrial curettage at 6 and 12 months; relapse reported in ≈ 22 % within 3 years. Despite microbiological cure, structural damage often persists. Research & Future Directions Novel diagnostics: Multiplex PCR panels, next-generation GeneXpert, cfDNA assays to improve sensitivity without sacrificing specificity. Endometrial regeneration: Pilot studies on mesenchymal stem cells, platelet-rich plasma, nano-carriers, and growth-factor scaffolds aim to reverse intra-uterine adhesions. Targeted therapeutics: Trials exploring shorter all-oral MDR regimens and immunomodulators (e.g., host-directed therapies) are ongoing. Key Take-Home Messages High index of suspicion is essential in women from endemic areas presenting with unexplained infertility or atypical menstrual disorders. Combined diagnostic strategy (histology + molecular testing + imaging) maximises detection in this paucibacillary disease. Early treatment yields excellent microbiological outcomes, but fertility restoration remains limited; prompt diagnosis before irreversible damage is crucial. Advanced reproductive techniques offer hope but success hinges on preserved endometrial function—highlighting the need for continued research into regenerative therapies. Selected References Sharma JB. Genital tuberculosis in females. Int J Reprod Med. 2017:1–9. Neonakis IK, et al. Female genital tuberculosis revisited. Eur J Clin Microbiol Infect Dis. 2020. Schaefer G. Tuberculosis of the female genital tract. GLOWM; updated 2022. ⚠️ Disclaimer: This content is intended for educational purposes only and should not substitute professional medical advice, diagnosis, or treatment. #Pathology #WomensHealth #MedicalEducation #NotasDePatologia #UterineTuberculosis #GenitalTuberculosis #MedicalEducation #NotasDePatologia
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aung phyo
aung phyo@pathphyo·
The beauty and the beast on FNAC breast! Upper one is benign epithelial cluster while the lower one is malignant epithelial cluster suggestive of invasive ductal carcinoma . #pathology #cytopath #IDC #FNAC
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aung phyo
aung phyo@pathphyo·
31 yrs old lady with right ovarian tumor. The gross and histologic patterns are consistent with stage IA dysgerminoma. #pathology #gynepath #dysgerminoma
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Sebastian Cruz Barbosa
Sebastian Cruz Barbosa@sebastianpathos·
30-year-old woman with ectopic pregnancy. Incidental finding on the tubal surface. #gynpath #pathology
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Simin
Simin@SiminSh5·
@ClinChemMD Thank you so much Professor 🙏🤩
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Riza B
Riza B@RizaBaiseitova1·
@SiminSh5 Congratulations 🔥🔥🔥
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Zahra Sarrafan Chaharsoughi, MD
Today, I was honored to present our work titled “Enhancing Digital Pathology: Reducing Blurred Images of Immunohistochemistry Slides through Staining Protocol Optimization” @UTMB_Pathology at the 10th Annual Quality Improvement and Patient Safety Poster Session.
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Gladell Paner, MD
Gladell Paner, MD@GladellPaner·
Tubulocystic renal tumor with a twist. 👀 What’s your top diagnosis #GUPath tweeps? #OnePicDx Answer in comment. 👇🏻👇🏻👇🏻
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Jay "Thymocyte" Hwang
Jay "Thymocyte" Hwang@Path4People·
When I first started residency, I thought "oh p16 block +... HPV infection!💡" Then I saw other non-HPV entities that were p16+ (eg liposarcoma) p16=a surrogate for HPV infection: E7 protein HPV -> inactivate RB -> p16 +++ But other tumors can also inactivate Rb -> p16+++
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