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61
MD : Medical Data : medicinska revija = medical review / glavni i odgovorni urednik Dušan Lalošević. - Vol. 1, no. 1 (2009)- . - Zemun : Udruženje za kulturu povezivanja Most Art Jugoslavija ; Novi Sad : Pasterovo društvo, 2009- (Beograd : Scripta Internacional). - 30 cm

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ISSN 1821-1585 = MD. Medical Data
COBISS.SR-ID 158558988


TIPIČNI KARCINOID I DIFUZNA IDIOPATSKA HIPERPLAZIJA PLUĆNIH NEUROENDOKRINIH ĆELIJA KOD PACIJENTKINJA OBOLELIH OD KARCINOMA DOJKE - PRIKAZ DVA SLUČAJA /

TYPICAL CARCINOID AND DIFFUSE IDIOPATHIC PULMONARY NEUROENDOCRINE CELL HYPERPLASIA IN PATIENT WITH BREAST CANCER - REPORTS OF TWO CASES

Authors

 

Bosiljka Krajnović Pavlović 1,2, Aleksandra Lovrenski 1,2, Tanja Lakić 1,4, Aleksandra Ilić 1,4, Siniša Maksimović 1,2, Milan Popović1,3, Dragana Tegeltija1,2

1Medicinski fakultet, Univerzitet u Novom Sadu, Republika Srbija
2Institut za plućne bolesti Vojvodine, Sremska Kamenica, Republika Srbija
3Institut za onkologiju Vojvodine, Sremska Kamenica, Republika Srbija
4Univerzitetski klinički centar Vojvodine, Novi Sad, Republika Srbija

 

UDK: 616.24-006.6
618.19-006.6-06


The paper was received / Rad primljen: 15.11.2023.

Accepted / Rad prihvaćen: 30.111.2023.

 


Correspondence to:


Dr Bosiljka Krajnović
Institut za plućne bolesti Vojvodine
Put doktora Goldmana 4
21208 Sremska Kamenica
Tel: 060 456 1630
e-mail: pavlovicbosiljka@yahoo.com

 

 

Sažetak

 

 

Uvod: DIPNECH (eng. diffuse idiopathic pulmonary neuroendocrine cell hyperplasia) predstavlja retko oboljenje koje može biti asimptomatsko ili se može manifestovati simptomima konstriktivnog bronhiolitisa - nedostatkom vazduha i nadražajnim kašaljem što može biti pogrešno protumačeno kao astma. Prikaz dva slučaja: Bolesnicama starosti 69 i 74 godina, sa istorijom operativno lečenog duktalnog karcinoma dojke i aktuelnim osećajem dispneje i nadražajnim kašljem, u sklopu redovnih onkoloških kontrola načinjena je kompjuterizovana tomografija pluća. Registrovane su višestruke nodularne promene koje su bile suspektne na metastaze primarnog  malignog oboljenja. Spirometrijskim pregledom verifikovan je lak opstruktivni poremećaj ventilacije. Nakon preoperativne pripreme urađena je hirurška intervencija (atipična resekcija gornjeg i srednjeg režnja desno kod prve i segmentektomija prvog segmenta levo kod druge pacijentkinje). Patohistološkom analizom nađene su linearne proliferacije uniformnih okruglastih ćelija fino dispergovanog jedarnog hromatina izgleda „so i biber“ iznad bazalne membrane bronhiolarne sluznice, morfoloških karakteristika DIPNECH-a. Pored toga nađu se područja opisanih ćelija sa invazijom bazalne membrane koje odgovaraju tumorletu (veličina <5mm) i karcinoidu (veličina >5mm) stadijuma IA. Imunohistohemijskom analizom (CD56, sinaptofizin, hromogranin: pozitivni; estrogen, progesteron, TTF-1, napsin A i GATA- 3: negativni) u oba slučaja potvrđena je neuroendokrina diferencijacija opisanih ćelija. Zaključak: DIPNECH se radiološki prezentuje kao noduli u plućnom parenhimu što klinički može pobuditi sumnju na metastasku bolest kod pacijenata sa ranije dijagnostikovanim malignim oboljenjem te se dijagnoza mora potvrditi bioptičkim uzorkom.

 

Ključne reči:

DIPNECH, karcinoid, tumorlet, neuroendokrine ćelije

 

 

 

Abstract

 

Intraduction: DIPNECH is a rare disease that may be asymptomatic or present with constrictive bronchiolitis symptoms- shortness of breath and irritating cough which can be misinterpreted as asthma. Outlines of cases: A 69-years-old and 74-years-old patients with surgically treated ductal breast cancer history and current dyspnea and irritable cough, underwent lung computed tomography as part of regular oncological follow-ups. Multiple noduli were registered that were suspicious for primary malignancy metastases. Spirometric examination verified mild obstructive ventilation disorder. After preoperative preparation, surgery was done (right upper and middle lobes atypical resection in the first and left segmentectomy of the first segment in the second patient). Pathohistological analysis revealed linear uniform round cells proliferations with finely dispersed nuclear chromatin with "salt and pepper" appearance above the bronchial mucosa basement membrane, morphological characteristics of DIPNECH. In addition, areas of the described cells with basal membrane invasion corresponding to the tumorlet (size <5mm) and carcinoid (size >5mm) stage IA were found. Immunohistochemical analysis (CD56, synaptophysin, chromogranin: positive; estrogen, progesterone, TTF-1, napsinA and GATA-3: negative) in both cases confirmed the neuroendocrine differentiation of the described cells. Conclusion: DIPNECH is a rare condition, and because of the imaging similarities it is difficult to distinguish it from metastic disease in the lung parenchyma. Therefore, as a part of routine practice, a definitive diagnosis of DIPNECH needs to be confirmed by tissue biopsy.

 


Key words:

DIPNECH, carcinoid, tumorlet, neuroendocrine cells

 

 

 

 

References:

  1. Travis WD, Brambilla E, Burke AP, Marx A, Nicholson AG. WHO classification of tumors of the lung, pleura, thymus and heart. 5th ed. Geneva: WHO Press; 2021.
  2. Aguayo SM, Miller YE, Waldron JA Jr., et al. Brief report: idiopathic diffuse hyperplasia of pulmonary neuroendocrine cells and airways disease. N Engl J Med 1992; 327: 1285-8.
  3. Rossi G, Cavazza A, Spagnolo P, Sverzellati N, Longo L, Jukna A, et al. Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia syndrome. Eur Respir J. 2016;47(6):1829-41. doi: 10.1183/13993003.01954-2015.
  4. Carmichael MG, Zacher LL. The demonstration of pulmonary neuroendocrine cell hyperplasia with tumorlets in a patient with chronic cough and a history of multiple medical problems. Mil Med. 2005;170(5):439-41. doi: 10.7205/milmed.170.5.439.
  5. Alves AP, Barroso A, Dias M. Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia: A Clinical Case. Eur J Case Rep Intern Med. 2020;7(3):001422. doi: 10.12890/2020_001422.
  6. Davies SJ, Gosney JR, Hansell DM, Wells AU, du Bois RM, Burke MM, Sheppard MN, Nicholson AG. Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia: an under-recognised spectrum of disease. Thorax. 2007;62(3):248-52. doi: 10.1136/thx.2006.063065.
  7. Hayes AR, Luong TV, Banks J, Shah H, Watkins J, Lim E,  et al. Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia (DIPNECH): Prevalence, clinicopathological characteristics and survival outcome in a cohort of 311 patients with well-differentiated lung neuroendocrine tumours. J Neuroendocrinol. 2022 Oct;34(10):e13184.
  8. Almquist DR, Sonbol MB, Ross HJ, Kosiorek H, Jaroszewski D, Halfdanarson T. Clinical characteristics of diffuse idiopathic pulmonary neuroendocrine cell hyperplasia: a retrospective analysis. Chest. 2021; 159(1): 432-434. 
  9. Sun TY, Hwang G, Pancirer D, et al. Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia: clinical characteristics and progression to carcinoid tumour. Eur Respir J. 2022; 59(1): 2101058.
  10. Mengoli MC, Rossi G, Cavazza A, Franco R, Marino FZ, Migaldi M, et al. Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia ( DIPNECH) syndrome and carcinoid tumors with/without NECH. AJSP 2018;42(5): 646-55.
  11. Nassar AA, Jaroszewski DE, Helmers RA, Colby TV, Patel BM, Mookadam F. Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia: a systematic overview. Am J Respir Crit Care Med. 2011 Jul 1;184(1):8-16.
  12. Lee JS, Brown KK, Cool C, Lynch DA. Diffuse pulmonary neuroendocrine cell hyperplasia: radiologic and clinical features. J Comput Assist Tomogr. 2002;26(2):180-4.
  13. Ge Y, Eltorky MA, Ernst RD, Castro CY. Diffuse idiopathc pulmonary neuroendocrine cell hyperplasia.  Ann Diagn Pathol 2007; 11:122-6.
  14. Myint ZW, McCormick J, Chauhan A, Behrens W, Anthony LB. Management of diffuse idiopathic pulmonary neuroendocrine cell hyperplasia: review and a single center experience. Lung. 2018;196(5):577–81.
  15. Mitchell PD, Kennedy MP, Henry MT. A Case of DIPNECH and Review of the Current Literature. OJRD. 2013;3(2):68-72.
  16. Warth A, Herpel E, Schmähl A, Storz K, Schnabel PA. Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia (DIPNECH) in association with an adenocarcinoma: a case report. J Med Case Rep. 2008;2:21.
  17. Killen H. DIPNECH presenting on a background of malignant melanoma: new lung nodules are not always what they seem. Case Reports 2014;2014:bcr2014203667.
  18. Lima Ferreira J, Marques B, Elvas A R, Simões de Carvalho F, Fonseca A L, Amaro T, et al. Medullary thyroid carcinoma and DIPNECH: an unexpected association. 17th Annual ENETS Conference for the Diagnosis and Treatment of Neuroendocrine Tumor Disease. 11-13 March 2020; Barcelona,Spain.
  19. Pedro J, Cunha FM, Neto V, Hespanhol V, Martins DF, Guimarães S, Varela A, Carvalho D. Coexistence of DIPNECH and carotid body paraganglioma: is it just a coincidence? Endocrinol Diabetes Metab Case Rep. 2020 May 13;2020:EDM19-0141.
  20. Chung, C.; Bommart, S.; Marchand-Adam, S.; Lederlin, M.; Fournel, L.; Charpentier, M.-C.; Groussin, L.; Wislez, M.; Revel, M.-P.; Chassagnon, G. Long-Term Imaging Follow-Up in DIPNECH: Multicenter Experience. J. Clin. Med. 2021, 10, 2950.

PDF: 09-Krajnović B. et al. MD-Medical Data 2022;15(3) 109-113.pdf

 

 

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