Sertoli-Cell-Only Syndrome


Article Author:
Kamleshun Ramphul
Hassam Zulfiqar


Article Editor:
Stephanie Mejias


Editors In Chief:
Stephen Leslie
Karim Hamawy


Managing Editors:
Avais Raja
Orawan Chaigasame
Carrie Smith
Abdul Waheed
Khalid Alsayouri
Trevor Nezwek
Radia Jamil
Patrick Le
Anoosh Zafar Gondal
Saad Nazir
William Gossman
Hassam Zulfiqar
Steve Bhimji
John Shell
Matthew Varacallo
Heba Mahdy
Ahmad Malik
Sarosh Vaqar
Mark Pellegrini
James Hughes
Beata Beatty
Nazia Sadiq
Hajira Basit
Phillip Hynes
Tehmina Warsi


Updated:
6/9/2019 12:45:01 AM

Introduction

Sertoli cell-only syndrome (SCO) is also known as Del Castillo syndrome and germ cell aplasia. Sertoli cells are found in the convoluted seminiferous tubules and form part of the blood-testis barrier in males. They also play an important role in spermatogenesis which is sperm production. The cells respond to a hormone called follicle-stimulating hormone (FSH) that is released by the hypothalamus.[1] Patients with Sertoli cell-only syndrome are typically males between ages 20 to 40. In Sertoli cell-only syndrome, only Sertoli cells line the seminiferous tubules of the testis, and the patients have very low or absent spermatogenesis. These patients are typically normal on physical examination as this condition presents with infertility without sexual abnormality. Diagnosis is usually made based on testicular biopsy findings. Most cases are multifactorial and idiopathic. Patients can still reproduce with assisted reproductive technology.

Etiology

Sertoli cells have multiple vital reproductive functions in males. They play an essential role in the proper growth and development of spermatogonia by secreting substances required for their growth and nourishment. Sertoli cells also secrete the anti-Mullerian hormone, AMH, that leads to the regression of Mullerian ducts in a male fetus. This hormone prevents the development of any internal female reproductive organs during the early stages of embryogenesis in a male fetus.

Sertoli cells also secrete inhibin-B which provides the down-regulatory effect of follicle-stimulating hormone secretion on the hypothalamus. Activin is another product secreted by Sertoli cells. It provides positive feedback on the hypothalamus for spermatogenesis and leads to a higher FSH level.

Epidemiology

There are no exact figures for the prevalence of this condition, but it is estimated that less than 5% to 10% of infertile men may be having Sertoli cell-only syndrome. They present with only infertility. While there is no racial predilection, it is slightly more common in Caucasian males. The most commonly affected age group involves adults of 20 to 40 years old.

Pathophysiology

Sertoli cell-only syndrome most likely is a multifactorial and idiopathic condition. The diagnosis is often made when young male patients come for an evaluation for infertility. They present with reduced or absent spermatogenesis and usually have a normal physical examination.

Multiple possible pathways may be involved in the pathogenesis of this condition. Researchers hypothesize that congenital absence of germ cells can result from proper failure of migration of gonocytes. The Yq11 region is also known as the azoospermia factor region (AZF region). Microdeletions in the Yq11 region of the Y chromosome, especially in the AZFb/b+c region, have been found in some patients with SCO syndrome and is another possible cause of the disease. Deletions between palindromes P5 and P1 and between P4 and P1 have also been reported. Yang et al. also hypothesized that two deletions in the interval region between P4 and P3 might also be involved in the pathophysiology of the condition. Apoptotic elimination and altered maturation of germ cells through mutations of Fas, FasL, and active caspase-3 have also been reported recently in the literature.[2][3][4][5]

The patients present with normal levels of luteinizing hormone (LH) and testosterone. The low level of inhibin-B leads to a higher than normal level of follicle-stimulating hormone (FSH). A study conducted by Stouffs et al. showed that in Caucasian males with SCO syndrome, karyotype abnormalities, such as Klinefelter syndrome, were the most common abnormality seen.[6]

The pathophysiology of the disease can be summarized as follows:

  • Mostly idiopathic
  • Genetic as discussed above
  • Toxin exposure leading to lower spermatogenesis
  • Radiation exposure to the testicular region
  • History of trauma leading to decreased sperm cell production
  • Viral infection

Histopathology

According to Nistal et al., histology of biopsies can vary. They can appear as normal mature cells, while others might present as involuting, immature, or dysgenetic. The shapes of the cell and nucleus as well as changes in the cytoplasm are helpful for categorizing them.[7]

History and Physical

The patients are typically young males, aged 20 to 40, who come for an infertility evaluation. The testes can be normal or smaller in size. They have a normal consistency and shape. Some patients have been reported to show atrophy of the testes. On physical examination, no gynecomastia is seen, and patients present with normal virilization. No other physical abnormalities are usually reported.

Evaluation

Most patients with Sertoli cell-only syndrome are further evaluated by conducting a semen analysis. Azoospermia, which refers to the absence of sperm, is often seen in such patients. A very small percentage of patients may still have a low detectable level of sperm.

Treatment / Management

At present, there is no treatment for Sertoli cell-only syndrome (SCO). However, for some cases, patients with very low sperm counts can still be considered for testicular sperm extraction (TESE). TESE allows removal of the sperm from the patient's testes and the sperm can be used to fertilize an egg via intracytoplasmic sperm injection (ICSI). Some studies have shown that the recovery is better with higher FSH levels in the blood.[8][9]

The rate of successfully retrieving the sperm varies. Multiple factors such as the presence of sperm cells can influence the outcome of TESE and ICSI. Some studies have even suggested that only 13% of patients with Sertoli cell-only syndrome successfully managed to have a child via these procedures.[10]

Couples are also advised to undergo genetic testing to confirm if the children could also be at risk of the condition.

Differential Diagnosis

It is vital to properly rule out other conditions that may present with a low sperm count. Some of the differentials to consider are:

  • Azoospermia 
  • Leydig cell hyperplasia
  • Klinefelter syndrome 
  • End-stage testis failure 
  • Hypospermatogenesis 

Prognosis

The prognosis of the patients in terms of fertility varies and in some cases assisted reproductive technology can help with reproduction.

Consultations

Patients should have proper follow-ups with their physicians. It is also strongly advised to avoid any gonadotoxins, such as chemotherapy, in order to preserve any remaining fertility.

Pearls and Other Issues

Sertoli cell-only (SCO) syndrome is a most often a multifactorial and idiopathic condition that leads to germ cells aplasia. Patients are sexually normal but have impaired spermatogenesis. Sperm analysis will usually show azoospermia. There are various techniques available to help patients who have some levels of sperms reproduce. The success rate, however, varies.

Enhancing Healthcare Team Outcomes

Sertoli cell only syndrome is best managed by a multidisciplinary team including nurses and pharmacists. While the diagnosis is not difficult the treatment is unsatisfactory for couples who want to conceive.

At present, there is no treatment for Sertoli cell-only syndrome (SCO). However, in some cases, patients with very low sperm counts can still be considered for testicular sperm extraction (TESE). TESE allows removal of the sperm from the patient's testes and the sperm can be used to fertilize an egg via intracytoplasmic sperm injection (ICSI). Some studies have shown that the recovery is better with higher FSH levels in the blood. However, patients need to be told that these procedures are prohibitively expensive and do not guarantee fertility.

Only about 10% of couples go on to conceive.


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Sertoli-Cell-Only Syndrome - Questions

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What age group will commonly be diagnosed with Sertoli-cell-only (SCO) syndrome?



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Which techniques can help patients with Sertoli-cell-only (SCO) syndrome reproduce?



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Which of the following can be involved in the pathophysiology of Sertoli-cell-only (SCO) syndrome?



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Which disease involves the Yq11 region, also known as the azoospermia factor region?



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A 27-year-old man comes to the clinic after having been unable to conceive with his wife. They have been trying for two years and decided to seek medical help. The man was normal on physical examination, with no gynecomastia and normal male sexual characteristics. His wife was also normal. Further examinations showed that he has microdeletions in the Y chromosome and germ cell aplasia causing his infertility. Which region is more likely to be affected on the Y chromosome?



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A 27-year-old man comes to the clinic for evaluation after having been unable to conceive with his wife. His testes are normal in size, shape, and consistency. No gynecomastia and other physical abnormalities are seen on physical examination. His Y chromosome shows microdeletions in the Yq11 region and the diagnosis of Sertoli cell-only syndrome is established. Which of the following findings will most likely correspond to the patient's diagnosis?



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Sertoli-Cell-Only Syndrome - References

References

Sharpe RM,McKinnell C,Kivlin C,Fisher JS, Proliferation and functional maturation of Sertoli cells, and their relevance to disorders of testis function in adulthood. Reproduction (Cambridge, England). 2003 Jun     [PubMed]
Yang Y,Ma MY,Xiao CY,Li L,Li SW,Zhang SZ, Massive deletion in AZFb/b c and azoospermia with Sertoli cell only and/or maturation arrest. International journal of andrology. 2008 Dec     [PubMed]
Ferlin A,Arredi B,Speltra E,Cazzadore C,Selice R,Garolla A,Lenzi A,Foresta C, Molecular and clinical characterization of Y chromosome microdeletions in infertile men: a 10-year experience in Italy. The Journal of clinical endocrinology and metabolism. 2007 Mar     [PubMed]
Hadjkacem-Loukil L,Hadj-Kacem H,Hadj Salem I,Bahloul A,Fakhfakh F,Ayadi H, Genotyping of Tunisian azoospermic men with Sertoli cell-only and maturation arrest. Andrologia. 2011 Jul 6     [PubMed]
Kim SK,Yoon YD,Park YS,Seo JT,Kim JH, Involvement of the Fas-Fas ligand system and active caspase-3 in abnormal apoptosis in human testes with maturation arrest and Sertoli cell-only syndrome. Fertility and sterility. 2007 Mar     [PubMed]
Stouffs K,Gheldof A,Tournaye H,Vandermaelen D,Bonduelle M,Lissens W,Seneca S, Sertoli Cell-Only Syndrome: Behind the Genetic Scenes. BioMed research international. 2016     [PubMed]
Ramasamy R,Lin K,Gosden LV,Rosenwaks Z,Palermo GD,Schlegel PN, High serum FSH levels in men with nonobstructive azoospermia does not affect success of microdissection testicular sperm extraction. Fertility and sterility. 2009 Aug     [PubMed]
Colpi GM,Colpi EM,Piediferro G,Giacchetta D,Gazzano G,Castiglioni FM,Magli MC,Gianaroli L, Microsurgical TESE versus conventional TESE for ICSI in non-obstructive azoospermia: a randomized controlled study. Reproductive biomedicine online. 2009 Mar     [PubMed]
Vloeberghs V,Verheyen G,Haentjens P,Goossens A,Polyzos NP,Tournaye H, How successful is TESE-ICSI in couples with non-obstructive azoospermia? Human reproduction (Oxford, England). 2015 Aug     [PubMed]
Nistal M,Jimenez F,Paniagua R, Sertoli cell types in the Sertoli-cell-only syndrome: relationships between Sertoli cell morphology and aetiology. Histopathology. 1990 Feb     [PubMed]

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